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Section 33

EurekaMag Full Text Articles Chapter 32,160



References:

Gasparini, P.; Borgato, L.; Piperno, A.; Gottardi, E.; Roetto, A.; Dianzani, I.; Pignatti, P.F.; Cappellini, M.D.; Fiorelli, G. 1992: Linkage analysis of highly polymorphic markers of 6p in Italian families with hereditary hemochromatosis. American Journal of Human Genetics 51(4 Suppl): A363
Durner, M.; Fu, D.; Greenberg, D.A.; Shinnar, S.; Resor, S.; Rosenbaum, D.; Kang, H.; Balaban Gil, K.; Labar, D.; Goldensohn, E.; Moshe, A.A.on Solomon; Klotz, R.; Dicker, E. 1997: Linkage analysis of idiopathic generalized epilepsy and chromosome 8 markers. Epilepsia 38(Suppl 8): 198
Whitehouse, W.; Rees, M.; Parker, K.; Sundqvist, A.; Chung, E.; Baralle, D.; Curtis, D.; Gardiner, R.M. 1993: Linkage analysis of juvenile myoclonic epilepsy Exclusion data for chromosome 6p including HLA. Cytogenetics and Cell Genetics 62(2-3): 87
Marazita, M.L.; Hart, T.C.; Kelson, T.; Burnmeister, J.A.; Schenkein, H.A.; Spence, J.E.; Nance, W.E. 1989: Linkage analysis of juvenile periodontitis jp with g6pd and pi. Cytogenetics and Cell Genetics 51(1-4): 1039
Hart, T.C.; Marazita, M.L.; Brooks, C.N.; Schenkein, H.A.; Diehl, S.R. 1991: Linkage analysis of juvenile periodontitis to chromosome 4q. Journal of Dental Research 70(Special Issue): 555
Sieving, P.; Bingham, E.; Roth, M.; Young, M.; Boehnke, M.; Kuo, S.; Ginsberg, D. 1989: Linkage analysis of juvenile x linked retinoschisis using four dna markers. American Journal of Human Genetics 45(4 Suppl): A161
Roses A.D.; Yamoaka L.; Gaskell P.C.; Bebout J.L.; Alberts M.J.; Haynes C.S.; Hung W Y.; Welch K.; Earl N.; Et Al 1990: Linkage analysis of late onset familial alzheimers disease. Neurobiology of Aging 11(3): 319
Sharp, J.; Savukoski, M.; Wheeler, R.B.; Harris, J.; Järvelä, I.; Peltonen, L.; Gardiner, M.; Williams, R. 1995: Linkage analysis of late-infantile neuronal ceroid-lipofuscinosis. American Journal of Medical Genetics 57(2): 348-349
Blossey, H.; Guo, S.W.; McKnight, B.; Tierney, C.; Thompson, E.; Wijsman, E. 1992: Linkage analysis of malignant melanoma with the chromosome 1 markers D1S47 and PND. Cytogenetics and Cell Genetics 59(2-3): 182-184
Hyde, C.A.; Fazzone, N.; Hudgins, L.; Sottile, T.R.Jr; Blanton, S.H.; Schwartz, R.C.; Young, M.; Sarfarazi, M.; Tsipouras, P. 1990: Linkage analysis of marfan syndrome investigation of decorin and fibrillar collagens as candidate molecules. Matrix 10(4): 241
Hudgins, L.; Hyde, C.A.; Sottile, T.R.Jr; Blanton, S.H.; Schwartz, R.C.; Sarfarazi, M.; Tsipouras, P. 1990: Linkage analysis of marfan syndrome with 47 markers. Pediatric Research 27(4 Part 2): 132A
Hirano, T.; Kobayashi, N.; Nakamaru, T.; Hara, K.; Sugimoto, Y. 1998: Linkage analysis of meat quality in Wagyu. Animal Genetics 29(Suppl 1): 64
Goldstein, A.M.; Bale, S.J.; Tucker, M.A. 1992: Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC. Cytogenetics and Cell Genetics 59(2-3): 203-205
Sherman, G.F.; Stone, L.V.; Galaburda, A.M.; Beier, D.R. 1997: Linkage analysis of neocortical ectopias in NXSM-D mice. Society for Neuroscience Abstracts 23(1-2): 1133
Kilpatrick, M.W.; Fullwood, P.; Farndon, P.A. 1989: Linkage analysis of nevoid basal cell carcinoma syndrome gorlin syndrome. American Journal of Human Genetics 45(4 Suppl): A146
Weissbecker, K.; Baxter, L.; Schwartz, J.; Sparkes, R.S.; Spence, M.A. 1989: Linkage analysis of obsessive compulsive disorder. Cytogenetics and Cell Genetics 51(1-4): 1105
Bernier, L.; Dewar, K. 1991: Linkage analysis of ophiostoma ulmi the causal agent of dutch elm disease. Canadian Journal of Plant Pathology 13(3): 271
Goonewardena, P.; Glicksman, A.; Brown, W.T. 1991: Linkage analysis of proximal dna markers rn1 and vk23 used in the diagnosis of fragile x syndrome. American Journal of Human Genetics 49(4 Suppl): 341
Mizoguchi, Y.; Hara, K.; Watanabe, T.; Fujikawa, A.; Suzuki, T.; Kikuchi, T.; Takahashi, T.; Kobayashi, N.; Tathuda, K.; Iwao, K.; Fujiwara, T.; Harada, K.; Kosugi, N.; Hirose, K.; Satoh, H.; Hara, Y.; Mizoshita, K.; Tanabe, Y.; Sugimoto, Y. 1998: Linkage analysis of quantitative trait loci in Wagyu cattle. Animal Genetics 29(Suppl 1): 64
Lutze, M.; Cox, N.J.; Brandt, C.R. 1991: Linkage analysis of rayleigh match range width and x chromosome markers. IOVS Investigative Ophthalmology and Visual Science 32(4): 1092
Freedman, B.I.; Yu, H.; Spray, B.J.; Rich, S.S.; Bowden, D.W. 1996: Linkage analysis of renin angiotensin axis candidate genes and end-stage renal disease in African Americans. Journal of the American Society of Nephrology 7(9): 1317
Muir W.; Blackwood D.; St Clair D.; Walker M.; Baillie D.; Hubbard A. 1991: Linkage analysis of schizophrenia with polymorphic loci on chromosome 11q. Cytogenetics and Cell Genetics 58(1-4): 1966-1967
Guanti G.; Stella A.; Origone P.; Susca F.; Lonoce A.; Gentile M.; Montera M.; Ponz De Leon M.; Sassatelli R.; Et Al 1991: Linkage analysis of six polymorphic markers mapping close to familial adenomatous polyposis gene. European Journal of Cancer 27(Suppl 3): S60
Nadkarni, N.; Ingraham, S.; Kole, J.; Didonato, C.; Rosenfeld, S.; Herta, N.; Hurko, O.; Hyser, C.; Florence, J. 1993: Linkage analysis of spinal muscular atrophy. Neurology 43(4 Suppl 2): A210
Tonin, P.; Ghadirian, P.; Lynch, H.; Lenoir, G.; Narod, S. 1995: Linkage analysis of the BRCA2 locus at chromosome 13q12-13 in hereditary breast cancer families. American Journal of Human Genetics 57(4 Suppl): A37
Auerbach, A.D.; Shin, H.T.; Kaporis, A.G.; Stevens, V.; Verlander, P.C. 1994: Linkage analysis of the Fanconi anemia gene FACC with chromosome 9q markers. American Journal of Human Genetics 55(3 Suppl): A179
Gibbs, M.; Mcindoe, R.A.; Stanford, J.L.; Jarvik, G.P.; Brandzel, S.; Neal, C.L.; Li, S.; Hood, L.; Goode, E.L.; Ostrander, E.A. 1997: Linkage analysis of the HPC1 region in high risk prostate cancer families. American Journal of Human Genetics 61(4 Suppl): A15
Koller, D.L.; Foroud, T.; Conneally, P.M.; Reed, T.; Edenberg, H.J.; Li, T.K. 1995: Linkage analysis of the MNS and esterase D chromosomal regions with alcohol dependence. American Journal of Human Genetics 57(4 Suppl): A324
Wada, H.; Maruse, K.; Shima, A. 1993: Linkage analysis of the Medaka using arbitrarily primed PCR. Zoological Science (Tokyo) 10(Suppl ): 78
Mcquitty, C.K.; Emala, C.W.; Levine, M.A.; Hirshman, C.A. 1993: Linkage analysis of the beta-2-adrenergic receptor gene in families with inherited asthma. Anesthesiology 79(3A): A1215
Allen, K.M.; Gleeson, J.G.; Ross, M.E.; Scheffer, I.; Berkovic, S.; Berg, M.; Motte, J.; Dobyns, W.B.; Walsh, C. 1996: Linkage analysis of the double cortex/ X-linked lissencephaly, a human mutation causing abnormal neuronal migration. Society for Neuroscience Abstracts 22(1-3): 519
Kumar, A.; Olson, T.M.; Thibodeau, S.M.; Michels, V.; Wallace, M.R. 1994: Linkage analysis of the elastin gene region in familial supravalvar aortic stenosis. Journal of the American College of Cardiology 1994(SPEC ISSUE): 305A
Tomita, Y.; Miyamura, Y.; Kohno, M.; Matsunaga, J. 1998: Linkage analysis of the gene for dyschromatosis symmetrica hereditaria-its locus is not on chromosome 9. Journal of Dermatological Science 16(Suppl 1): S150
Onozuka, H.; Noguchi, M.; Mikami, T.; Satoh, H.; Hashimito, M.; Yasuda, H.; Wakisaka, A. 1991: Linkage analysis of the gene for familial hypertrophic cardiomyopathy. Japanese Circulation Journal 55(Suppl A): 310-311
Nakamura, A.; Komatsu, S.; Xia, B.S.; Hirano, H. 1995: Linkage analysis of the gene loci for seed glutelin , semidwarfism and shattering habit in rice. Breeding Science 45(2): 185-188
Bu, X.; Warden, C.H.; Xia, Y.R.; De Meester, C.; Puppione, D.L.; Teruya, S.; Lokensgard, B.; Daneshmand, S.; Brown, J.; Gray, R.J. 1994: Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition: evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein loci. Human Genetics 93(6): 639-648
Farndon, P.A.; Fullwood, P.; Hardy, C.; Kilpatrick, M.W. 1991: Linkage analysis of the naevoid basal cell carcinoma nbccs syndrome. Cytogenetics and Cell Genetics 58(1-4): 2112
Goldstein, A.M.; Bale, S.J. 1991: Linkage analysis of the nevoid basal cell carcinoma syndrome nbccs. Cytogenetics and Cell Genetics 58(1-4): 1853
Wu, J.M.; Hargrave, P.; Wakeland, E.K. 1994: Linkage analysis of the polygenic inheritance of humoral immunity to HEL and rhodopsin. FASEB Journal 8(4-5): A526
Weaver, E.J.; King, R.A.; Norris, K.; Knobloch, W.H.; Shamban, A.; Jimenez, S.A.; Prockop, D.J.; Knowlton, R.G. 1989: Linkage analysis of the type ii collagen gene col2a1 and hereditary arthro ophthalmopathy aom in three large families. Cytogenetics and Cell Genetics 51(1-4): 1103
Yamazaki, H.; Nakagawa, Y.; Saito, A.; Nishi, S.; Sakatsume, M.; Meguro, H.; Takeda, T.; Arakawa, M. 1993: Linkage analysis of thin basement membrane disease and type IV collagen alpha-3 and alpha-4 chain genes. Journal of the American Society of Nephrology 4(3): 827
Long, J.C.; Hesselbrock, D.; Urbanek, M.; Robin, R.; Goldman, D. 1998: Linkage analysis of three chromosome 4 microsatellites and ADH to alcoholism in an American Indian population. Alcoholism Clinical and Experimental Research 22(3 ABSTR Suppl ): 97A
Thakker, R.V.; Wooding, C.; Parkinson, D.B.; Blake, D.; Whyte, M.P.; Davies, K.E. 1991: Linkage analysis of three cloned dna sequences dxs294 cdr and dxs105 in x linked recessive hypoparathyroid families. Cytogenetics and Cell Genetics 58(1-4): 2087
Mccombs, S.D.; Saul, S.H. 1992: Linkage analysis of three new alleles affecting puparium morphology in the oriental fruit fly, Bactrocera dorsalis. Annals of the Entomological Society of America 85(6): 799-804
Koeleman, B.P.C.; Krommenhoek Van Es, T.; Sandkuijl, L.A.; Reitsma, P.H.; Bertina, R.M. 1994: Linkage analysis of thrombotic disease in 15 clinically dominant protein C deficient families. British Journal of Haematology 87(Suppl 1): 196
Povey S.; Attwood J.; Burley M.; Lovegrove J.; Whitehouse D.; Fryer A.E.; Osborne J.; Al Gazali L.; Mueller R.F.; Et Al 1989: Linkage analysis of tuberous sclerosis in english families. Cytogenetics and Cell Genetics 51(1-4): 1061
Van Broeckhoven C.; Backhovens H.; Van Hul W.; Wehnert A.; Verniers H.; De Winter G.; Bruyland M.; Gheuens J.; Martin J.J.; Vandenberghe A. 1989: Linkage analysis of two extended alzheimer families with chromosome 21 dna markers. Cytogenetics and Cell Genetics 51(1-4): 1096
Pascal, O.; O'neill A.; Lefevre, M.; Moisan, J.P.; Bouhour, J.B. 1991: Linkage analysis of two families of hypertrophic cardiomyopathy. Journal of Cellular Biochemistry Suppl (15 Part C): 189
Smith, R.J.H.; Daiger, S.P.; Pelias, M.Z.; Kimberling, W.J.; Herrera, C.H.; Hejtmancik, J.F. 1991: Linkage analysis of usher syndrome in the louisiana acadian population clinical and genetic heterogeneity. American Journal of Human Genetics 49(4 Suppl): 360
Weston, M.D.; Kimberling, W.J.; Temp, M. 1989: Linkage analysis of usher syndrome with markers on chromosome 1. American Journal of Human Genetics 45(4 Suppl): A68
Lagerstrom, M.; Dahl, N.; Iselius, L.; Backman, B.; Pettersson, U. 1989: Linkage analysis of x linked amelogenesis imperfecta. Cytogenetics and Cell Genetics 51(1-4): 1028
Zhu, D.; Brown, D.R.; Mitchell, T.N.; Maumenee, I.H. 1991: Linkage analysis of x linked ocular albinism oa1. American Journal of Human Genetics 49(4 Suppl): 364
Inana, G.; Iwata, T.; Mashima, Y.; Sasabe, T.; Jacobson, S.G.; Murphey, W.H.; Litt, M.; Weleber, R.G. 1991: Linkage analysis of x linked retinitis pigmentosa families with ornithine aminotransferase oat related and other x short arm markers. American Journal of Human Genetics 49(4 Suppl): 344
Iwata, T.; Mashima, Y.; Sasabe, T.; Jacobson, S.G.; Weleber, R.G.; Murphey, W.H.; Inana, G. 1991: Linkage analysis of x linked retinitis pigmentosa using ornithine aminotransferase complementary dna l128 and otc probes. IOVS Investigative Ophthalmology and Visual Science 32(4): 1136
Morris, D.J.; Berkowtiz, D.E.; Dunn, D.S.; Hull, P.; Jenkins, T. 1989: Linkage analysis on chromosome 13q using families with an inherited skin disorder. Cytogenetics and Cell Genetics 51(1-4): 1048
Greenberg, D.A.; Durner, M.; Shinnar, S.S.; Resor, S.R.; Rosenbaum, D.; Cohen, J.; Kang, H.; Moshe, S.L.; Harden, C.; Yohai, D.; Balaban Gil, K.; Nadkarni, M.A. 1998: Linkage analysis on chromosome 6 shows evidence for heterogeneity within the JME syndrome. Epilepsia 39(Suppl 6): 144-145
Davis, M.B.; Ahmed, F.; Waddy, H.M.; Oley, C.; Harding, A.E. 1991: Linkage analysis on chromosome 9. Cytogenetics and Cell Genetics 58(1-4): 1937
Thomas, A. 1994: Linkage analysis on complex pedigrees by simulation. Ima Journal of Mathematics Applied in Medicine and Biology 11(2): 79-93
John, S.; Myerscough, A.; Marlow, A.; Ollier, W.; Silman, A.; Worthington, J. 1996: Linkage analysis studies of candidate genes in affected SIB pair RA families. British Journal of Rheumatology 35(ABSTR Suppl 1): 190
Wadelius, C.; Sjoholm, A.; Goonewardena, P.; Nilsson, L.A.; Cuijper, E.J.; Tijssen, C.C.; Tranebjerg, L.; Niesen, H.E.; Spath, P.; Pettersson, U. 1989: Linkage analysis suggest location of the properdin deficiency gene on the proximal part of the p arm of the x chromosome. Cytogenetics and Cell Genetics 51(1-4): 1100
Neibergs, H.L.; Homeister, A.; Rotter, J.I.; Pressman, S.; Yang, H. 1997: Linkage analysis supports NRAMP as a major susceptibility locus for ulcerative colitis. American Journal of Human Genetics 61(4 Suppl): A53
Naom, I.; D'alessandro, M.; Topaloglu, H.; Sewry, C.; Helbing Leclerc, A.; Guicheney, P.; Dubowitz, V.; Muntoni, F. 1996: Linkage analysis to the alpha-2 laminin locus on chromosome 6q2 in merosin-deficient congenital muscular dystrophy. European Journal of Human Genetics 4(Suppl 1): 1
Greenberg, D.A.; Hodge, S.E. 1989: Linkage analysis under "random" and "genetic" reduced penetrance. Genetic Epidemiology 6(1): 259-264
Sham, P.; Zhao, J. 1998: Linkage analysis using affected sib-pairs. Bishop, M J Guide to human genome computing, Second edition 75-88
Hart, T.C.; Marazita, M.L.; Burmeister, J.A.; Schenkein, H.A.; Nance, W.E.; Diehl, S.R. 1989: Linkage analysis using dna markers and hla association for juvenile periodontitis. American Journal of Human Genetics 45(4 Suppl): A142
Hellerqvist, C.G. 1990: Linkage analysis using Lindberg method. Methods in Enzymology 193: 554-573
Gray, G.R. 1990: Linkage analysis using reductive cleavage method. Methods in Enzymology 193: 573-587
Satler, C.; Walsh, E.; Korf, B.; Nadal Ginard, B. 1992: Linkage analysis with H-ras-1 probe identifies genetic heterogeneity of the long QT syndrome. Circulation 86(4 Suppl 1): I348
Kong, A.; Frigge, M.; Cox, N.; Wong, W.H. 1992: Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling. Cytogenetics and Cell Genetics 59(2-3): 208-210
Hegele R.A.; Wu L.L.; Hopkins P.N.; Lalouel J.M.; Williams R.R. 1990: Linkage analysis with candidate genes in familial obesity. Clinical Research 38(2): 536A
Lalle, P.; Stoppa Lyonnet, D.; Mazoyer, S.; Narod, S.A.; Rio, P.; Jamot, B.; Courjal, F.; Dutrillaux, B.; Bignon, Y.J.; Sobol, H. 1992: Linkage analysis with chromosome 17q marker in 19 French breast cancer and breast ovarian cancer syndrome families and possible relationship to other carcinomas. Breast Cancer Research and Treatment 23(1-2): 174
Rice, J.; Suarez, B.K.; Hampe, C.L.; Neuman, R. 1989: Linkage analysis with fixed prevalence: application to simulated data. Progress in Clinical and Biological Research 329: 165-170
Van Eerdewegh, P. 1989: Linkage analysis with inbreeding. Genetic Epidemiology 6(1): 277-279
Reis, A.; Kuester, W.; Linss, G.; Fuhrmann, W.; Wolff, G.; Gustafson, G.; Kuklik, M. 1991: Linkage analysis with microsatellite dna polymorphisms in basal cell nevus syndrome bcns. American Journal of Human Genetics 49(4 Suppl): 356
Grifa, A.; Totaro, A.; Carella, M.; Roetto, A.; Sbaiz, L.; Camaschella, C.; Gasparini, P. 1996: Linkage analysis with the new marker F22 in hereditary hemochromatosis families. European Journal of Human Genetics 4(Suppl 1): 90
Rowe, P.S.N.; Goulding, J.; Read, A.; Mountford, R.; Hanauer, A.; Oudet, C.; Meier Ewart, S.; Lehrach, H.; Davies, K.E.; O'riordan, J.L.H. 1993: Linkage analysis, and physical mapping of X-linked hypophosphataemic rickets. Calcified Tissue International 52(Suppl 1): S58
Torra, R.; Badenas, C.; Darnell, A.; Nicolau, C.; Revert, L.; Estivill, X. 1996: Linkage analysis, clinical features and prognosis of autosomal dominant polycystic kidney disease types 1 and 2. Nephrology Dialysis Transplantation 11(6): A63
Summar, M.L.; Desouki, M.; Schofield, J.P. 1995: Linkage and FISH analysis of the human carbamyl phosphate synthetase I gene and its reassignment to 2q35. Gastroenterology 108(4 Suppl): A1180
Yang, H.; Ohmen, J.D.; Ma, R.; Li, Z.; Bentley, L.G.; Targan, S.R.; Fischel Ghodsian, N.; Rotter, J.I. 1998: Linkage and association between Crohns disease and a putative locus on chromosome 12. Gastroenterology 114(4 Part 2): A1119
Rowe, R.E.; Wapelhorst, B.; Bell, G.I.; Risch, N.; Spielman, R.S.; Concannon, P. 1995: Linkage and association between insulin-dependent diabetes mellitus susceptibility and markers near the glucokinase gene on chromosome 7. Nature Genetics 10(2): 240-242
Chagnon, Y.C.; Perusse, L.; Chung, W.K.; Chagnon, M.; Leibel, R.L.; Bouchard, C. 1998: Linkage and association between the leptin receptor LEPR gene and human body composition in the Quebec Family Study. International Journal of Obesity 22(Suppl 3): S72
Bray, M.S.; Boerwinkle, E.; Hanis, C.L. 1996: Linkage and association of glucagon-like peptide with obesity and related measures among Mexican Americans in Starr County, Texas. American Journal of Human Genetics 59(4 Suppl): A249
Pound, S.E.; Pignatelli, P.M.; Macnicol, A.M.; Carothers, A.D.; Watson, M.L.; Wright, A.F. 1991: Linkage and association studies in adult onset polycystic kidney disease pkd1. Cytogenetics and Cell Genetics 58(1-4): 2117
Garenc, C.; Gagnon, J.; Perusse, L.; Chagnon, Y.C.; Despres, J.P.; Bergeron, J.; Leon, A.S.; Rao, D.C.; Skinner, J.S.; Wilmore, J.H.; Bouchard, C. 1998: Linkage and association studies of the lipoprotein lipase SER447TER mutation The HERITAGE Family Study. Medicine and Science in Sports and Exercise 30(5 Suppl): S7
John, S.L.; Hajeer, A.H.; Marlow, A.; Ollier, W.E.R.; Silman, A.; Worthington, J. 1996: Linkage and association studies of the natural resistance associated macrophage protein locus in rheumatoid arthritis. British Journal of Rheumatology 35(ABSTR Suppl 1): 188
Shastry, B.S.; Hejtmancik, J.F.; Plager, D.A.; Hartzer, M.K.; Trese, M.T. 1995: Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy. Genomics 27(2): 341-344
Bareil, C.; Schmitt Bernard, C.F.; Arnaud, B.; Claustres, M.; Hamel, C.; De Meeus, A. 1997: Linkage and candidate genes analysis in a family with X-linked incomplete type congenital stationary night blindness. American Journal of Human Genetics 61(4 Suppl): A266
Thirukkumaran, P.; Sawicki, M.P.; Gratton, K.J.; Johnson, C.J. 1995: Linkage and clinical analysis in the identification of high risk family members with multiple endocrine neoplasia 1. American Journal of Human Genetics 57(4 Suppl): A304
Jordan, S.A.; Mcguire, R.E.; Sullivan, L.S.; Gannon, A.M.; Humphries, P.; Daiger, S.P. 1994: Linkage and clinical characterization of families with the RP10 form of autosomal dominant retinitis pigmentosa. American Journal of Human Genetics 55(3 Suppl): A189
Messiaen, L.; Callens, T.; De Bie, S.; Schiaffino, V.; Bassi, M.; Ballabio, A.; De Paepe, A. 1995: Linkage and deletion analysis in a large 4-generation Belgian family with X-linked ocular albinism of the Nettleship-Falls type. American Journal of Human Genetics 57(4 Suppl): A198
Polumbo, P.A.; Hughes, A.L.; Dierwechter, L.M.; Whitesides, L.D.; Summar, M.L.; Tiller, G.E. 1994: Linkage and evolutionary relationships of the genes for human clotting factors VII and X. American Journal of Human Genetics 55(3 Suppl): A162
Saeed, A.; Ratnayake Lecamwasam, M.; Detrich, H.W.IIi 1997: Linkage and expression of the alpha- and beta-globin genes of Antarctic and temperate notothenioid fish. Molecular Biology of the Cell 8(Suppl ): 430A
Lehesjoki A E.; Sistonen P.; Rasi V.; De La Chapelle A. 1989: Linkage and gene order studies in hemophilia a. Cytogenetics and Cell Genetics 51(1-4): 1031
Morissette, J.; Harley, H.G.; Korneluk, R.G.; Plante, M.; Mathieu, J.; Thibault M C. 1991: Linkage and gene order studies in myotonic dystrophy. Cytogenetics and Cell Genetics 58(1-4): 2022
Labuda, M.C.; Otten, K.; Egeland, J.A.; Allen, C.; Pauls, D.L.; Gerhard, D.S. 1995: Linkage and haplotype analyses of bipolar affective disorder in the Old Order Amish. American Journal of Human Genetics 57(4 Suppl): A325
Ayyagari, R.; Smith, R.J.H.; Polymeropoulos, M.; Chinault, A.C.; Daiger, S.; Pelias, M.Z.; Wozencraft, L.; Kaiser Kupfer, M.; Hejtmancik, J.F. 1994: Linkage and haplotype analysis and physical mapping of the USH1C gene. IOVS Investigative Ophthalmology and Visual Science 35(4): 2143
Hurko, O.; Polymeropoulos, M.H.; Hsu, F.; Rubenstein, J.; Basnet, S.; Lane, K.; Dietz, H.; Spetzler, R.F.; Rigamonti, D. 1996: Linkage and haplotype analysis of autosomal dominant cavernous hemangiomas of the brain in four Mexican-American families. Neurology 46(2 Suppl): A172
Lennon, F.; Gaskell, P.C.; Wolpert, C.; Aylsworth, A.S.; Malin, D.; Warner, C.; Farrell, C.D.; Boustany, R.N.; Albright, S.G.; Kingston, H.M.; Cummings, W.J.K.; Hogan, E.L.; Vance, J.M.; Pericak Vance, M.A. 1995: Linkage and heterogeneity in hereditary spastic paraparesis. American Journal of Human Genetics 57(4 Suppl): A217
Short, M.P.; Haines, J.L.; Bove, C.; Henske, E.P.; Guillemette, W.; Sitsma, M.; Amos, J.; Andermann, E.; Gusella, J.F.; Kwiatkowski, D.J. 1992: Linkage and heterogeneity in tuberous sclerosis Linkage to chromosome 16 and resolution of old problems. American Journal of Human Genetics 51(4 Suppl): A201
Engle, E.C.; Wang, S.M.; Zwaan, J.T.; Mullaney, P.B.; Jabak, M.H.; Beggs, A.H. 1997: Linkage and homozygosity mapping of a variant of congenital fibrosis of the extraocular muscles to chromosome 11q131. American Journal of Human Genetics 61(4 Suppl): A30
Eggers, H.J.; Weyer, J.J. 1991: Linkage and independence of AIDS and Kaposi disease: the interaction of human immunodeficiency virus and some coagents. Infection 19(2): 115-122
Li, X.; Wistow, G.J.; Piatigorsky, J. 1994: Linkage and intergenic spacer of the duck delta-crystallin genes. IOVS Investigative Ophthalmology and Visual Science 35(4): 1706
Pandolfo M.; Cocozza S.; Cavalcanti F.; Antonelli A.; Campanella G.; De Michele G.; Di Donato S.; Filla A.; Pianese L.; Et Al 1992: Linkage and linkage disequilibrium in friedreichs disease possible association between genetic markers and onset ages. Neurology 42(4 Suppl 3): 392
Risch, N.; Claus, E.; Giuffra, L. 1989: Linkage and mode of inheritance in complex traits. Progress in Clinical and Biological Research 329: 183-188
Martell, K.J.; Weber, W.W. 1991: Linkage and molecular characteristics of monomorphic and polymorphic murine n acetyltransferases. FASEB Journal 5(4): A847
Ciaranello, R.D. 1996: Linkage and molecular genetics of infantile autism. Watson, S J Biology of schizophrenia and affective disease 129-161
Koty, P.P.; Marks, H.G.; Turel, A.; Flagler, D.; Angelini, C.; Pegoraro, E.; Vancott, A.C.; Manchester, D.; Zonana, J.; Bird, T.D.; Hoffman, E.P. 1994: Linkage and mutation analysis of Thomsen and Becker myotonia families. American Journal of Human Genetics 55(3 Suppl): A227
Sarfarazi, M.; Child, A.; Stailova, D.; Brice, G.; Coakes, R.; Crick, R.P. 1997: Linkage and mutation studies of adult-onset primary open angle glaucoma with TIGR and genes on 4 other chromosomes. American Journal of Human Genetics 61(4 Suppl): A402
Graham, J.M.Jr; Hixon, H.; Bacino, C.A.; Daack Hirsch, S.; Stadler, S.; Murrray, J.C. 1994: Linkage and physical mapping approaches utilizing families and individuals with a Goldenhar phenotype. American Journal of Human Genetics 55(3 Suppl): A370
Janson, M.; Larsson, C.; Nordenskjold, M.; Weber, G. 1991: Linkage and physical mapping of the men1 gene. American Journal of Human Genetics 49(4 Suppl): 123
Janson, M.; Larsson, C.; Weber, G.; Werelius, B.; Nordenskjold, M. 1991: Linkage and physical mapping of the men1 region on 11q13. Cytogenetics and Cell Genetics 58(1-4): 1964-1965
Antonarakis, S.E.; Blouin, J.L.; Curran, M.; Luebbert, H.; Kazazian, H.H.; Dombroski, B.; Housman, D.; Ton, C.; Karayiorgou, M.; Chakravarti, A.; Wolyniec, P.; Lasseter, V.K.; Nestadt, G.; Pulver, A.E. 1996: Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32. American Journal of Human Genetics 59(4 Suppl): A210
Filie, J.D.; Kozak, C.A. 1996: Linkage and synteny homologies between human chromosome 13 and mouse chromosomes 5, 8 and 14. Cytogenetics and Cell Genetics 75(2-3): 107
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Krajinovic, M.; Pinamonti, B.; Sinagra, G.; Vatta, M.; Severini, G.M.; Milasin, J.; Falaschi, A.; Camerini, F.; Giacca, M.; Mestoni, L.; Group, H.M. Disease Study 1996: Linkage of autosomal dominant familial dilated cardiomyopathy to chromosome 9. Journal of the American College of Cardiology 27(2 Suppl A): 226A
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Andersen, A. 1992: Linkage of census records a resource in occupational cancer studies. Revue d'Epidemiologie et de Sante Publique 40(Suppl 1): S102
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Nechiporuk, A.; Fain, P.; Kort, E.; Nee, L.E.; Frommelt, E.; Polinsky, R.J.; Korenberg, J.R.; Pulst, S.M. 1993: Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores. American Journal of Medical Genetics 48(1): 63-66
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Timmerman, J.M.; Levy, R. 1997: Linkage of foreign carrier protein or GM-CSF to a tumor antigen improves the efficacy of pulsed dendritic cell vaccination. Blood 90(10 Suppl 1 Pt 1): 514A
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Umeda, T.; Haneda, K.; Harauchi, H.; Inamura, K. 1998: Linkage of plural numbers of existed radiotherapy databases to an integrated multi-institutional radiation oncology database. Lemke, H U, Vannier, M W, Inamura, K, Farman, A G International Congress Series; CAR '98: Computer assisted radiology and surgery 282-288
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Hing, A.; Helms, C.; Burgess, A.; Wang, J.C.; Liu, L.; Lacy, M.; Slaugh, R.; Dowton, S.B.; Donis Keller, H. 1994: Linkage of preaxial polydactyly type II within human chromosome 7q36. American Journal of Human Genetics 55(3 Suppl): A188
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Hosoi, K.; Fujishita, M.; Shioda, Y.; Kodama, A.; Sugita, K.; Kurihara, K.; Murai, T.; Ueha, T. 1989: Linkage of purinergic receptors and egf receptors. Japanese Journal of Physiology 39(Suppl): S39
Hazra, D.K.; Lahiri, V.L.; Chaturvedi, G.K.; Khanna, P.; Saran, S. 1990: Linkage of radiogold to immunoglobulins as candidate isotopes for radioimmunotherapy. European Journal of Cancer 26(9): 1020
Durham, R.; Moore, G.; Guy, C. 1990: Linkage of restriction fragment length polymorphisms and isozymes in a backcross of citrus and poncirus. HortScience 25(9): 1154
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Kohn, E.C.; Felder, C.C.; Jacobs, W.; Holmes, K.A.; Day, A.; Freer, R.; Liotta, L.A. 1993: Linkage of selected signal transduction pathways with tumor cell proliferation. Proceedings of the American Association for Cancer Research 34: 85
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Sobanov, Y.ri; Glienke, Jens; Brostjan, Christine; Lehrach, Hans; Francis, Fiona; Hofer, Erhard 1998: Linkage of the CD94 and NKG2 genes to D12S77 in the human natural killer gene complex. Natural Immunity 16(2-3): 78
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Parker, J.D.; Woodruff, T.J.; Akinbami, L.J.; Kravets, N. 2008: Linkage of the US National Health Interview Survey to air monitoring data: an evaluation of different strategies. Environmental Research 106(3): 384-392
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Pras, E.; Aksentijevich, I.; Gruberg, L.; Prosen, L.; Dean, M.; Pras, M.; Kastner, D. 1992: Linkage of the gene for familial mediterranean fever to the short arm of chromosome 16. Journal of Cellular Biochemistry Suppl (16 Part F): 22
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Mietus Snyder, M.; Korf, B.; Ladias, J.A.; Karathanasis, S.K. 1989: Linkage of the human apolipoproteins a1 c3 a4 and the neural cell adhesion molecule ncam genes. Cytogenetics and Cell Genetics 51(1-4): 1044
Hager, J.; Clement, K.; Garner, C.; Philippi, A.; Jury, C.; Ldeduc, C.; Cardon, L.; Guy Grant, B.; Demenais, F.; North, N.; Froguel, P. 1996: Linkage of the human ob gene region to extreme obesity. European Journal of Human Genetics 4(Suppl 1): 147
Baldwin, C.T.; Hoth, C.; Amos, J.A.; Silva, E.O.D.; Milunsky, A. 1992: Linkage of the hup2 gene on chromosome 2q35 37 with waardenburg syndrome ws in a large brazilian family. Pediatric Research 31(4 Part 2): 130A
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Ray, K.; Baldwin, V.J.; Acland, G.M.; Aguirre, G.D. 1994: Linkage of the point mutation at the 807 codon in canine PDE-beta to rcd1 in Irish Setter dogs. IOVS Investigative Ophthalmology and Visual Science 35(4): 1611
Baker, M.A.; Ohlsson Wilhelm, B.M.; Carpenter, D.C.; Lorinc, R.L.; Gray, B.D.; Muirhead, K.A. 1994: Linkage of therapeutics to lipophilic agents enhances biological activity and binds tumor cells in vivo. Proceedings of the American Association for Cancer Research 35: 418
Buzza, M.; Wilson, D.; Savige, J. 1998: Linkage of thin basement membrane disease to the loci for X-linked and autosomal recessive Alport syndrome. Journal of the American Society of Nephrology 9(Program and Abstr. Issue): 387A
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George, J.B.; Li, D.; Zelenski, N.; Hui, F.; Garrard, W.T. 1996: Linkage of variable and joining gene segments in the murine immunoglobulin kappa locus. FASEB Journal 10(6): A1171
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Hauber, D.P.; Cavallo, J. 1991: Linkage relationships among electrophoretic gene loci in youngia japonica. American Journal of Botany 78(6 Suppl): 94
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Denton, M.J.; Keith, C.G.; Chen, J.D. 1989: Linkage relationships between an atypical form of x linked retinitis pigmentosa and a number of xp markers. Cytogenetics and Cell Genetics 51(1-4): 987
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Warner, T.T.; Davis, M.B.; Conway, D.; Fletcher, N.A.; Ahmad, F.; Marsden, C.D.; Harding, A.E. 1992: Linkage studies for chromosome 9Q32-34 in British families with idiopathic torsion dystonia. Journal of Neurology Neurosurgery and Psychiatry 55(12): 1215-1216
Northrup, H.; Blanton, S.H. 1991: Linkage studies for markers on 9q to tuberous sclerosis. Annals of the new York Academy of Sciences 615: 384-385
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Ben Hamida, M.; Hentati, F.; Blel, S.; Lennon, F.; Roses, A.D.; Vance, M.A.P.ricak; Vance, J.M. 1992: Linkage studies in Charcot-Marie-Tooth disease type 1 autosomal recessive. American Journal of Human Genetics 51(4 Suppl): A360
Lauteala, T.; Savontaus, M.L.; Simell, O.; Aula, P. 1996: Linkage studies in Finnish Lysinuric protein intolerance families. European Journal of Human Genetics 4(Suppl 1): 64
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Pulkkinen, L.; Christiano, A.M.; Uitto, J. 1993: Linkage studies in PXE families using RFLPs in candidate genes involved in elastic fiber assembly. Journal of Investigative Dermatology 100(4): 517
San Millan, J.L.; Viribay, M.; Peral, B.; Weissenbach, J.; Moreno, F. 1994: Linkage studies in Spanish autosomal dominant polycystic kidney disease-type 2 families. American Journal of Human Genetics 55(3 Suppl): A202
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Trump, D.; Whyte, M.P.; Wooding, C.; Pang, J.T.; Kocher, D.; Thakker, R.V. 1994: Linkage studies in a kindred from Oklahoma, with familial benign hypocalciuric hypercalcaemia and increasing serum parathyroid hormone concentrations indicate genetic heterogeneity and a third locus for FBH. Journal of Endocrinology 140(Suppl ): ABSTRACT P25
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Dion, F.; Barden, N.; Rouleau, G.A. 1992: Linkage studies in a large manic depressive illness kindred. American Journal of Human Genetics 51(4 Suppl): A362
Kruse, T.A.; Byskov, A.; Oftedal, G.; Wirsching, J.; Lovseth, T.W.; Gedde Dahl, T.Jr 1991: Linkage studies in a norwegian spastic paraplegia 2 family. Cytogenetics and Cell Genetics 58(1-4): 2071
Mcparland, P.; Papiha, S.S.; Gale, M.; Ward, M.; Bhattacharya, S.S. 1989: Linkage studies in adult polycystic kidney disease the question of genetic heterogeneity in northern england uk. Cytogenetics and Cell Genetics 51(1-4): 1042
Gasser, T.; Wszolek, Z.K.; Ozelius, L.; Lee, C.; Calne, D.; Breakeffield, X.O. 1992: Linkage studies in autosomal dominant Parkinsons disease. American Journal of Human Genetics 51(4 Suppl): A363
Padberg, G.W.; Wijmenga, C.; Brants, R.R.; Brouwer, O.F.; Sandkuijl, L.A. 1991: Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophy. Neurology 41(3 Suppl 1): 349
Speer, M.C.; Pericak Vance, M.A.; Gilchrist, J.M.; Yamaoka, L.H.; Hung W Y.; Roses, A.D. 1989: Linkage studies in autosomal dominant limb girdle muscular dystrophy. Cytogenetics and Cell Genetics 51(1-4): 1083
Casley, W.L.; Abdalla, J.A.; Armstrong, H.A.; Hudson, A.J.; Ebers, G.C. 1992: Linkage studies in autosomal dominant myotonia congenita thomsens disease admc. Neurology 42(4 Suppl 3): 282
Gedde Dahl, T.; Andresen, P.A.; Jonassen, R.; Anton Lamprecht, I.; Myklebost, O.; Olaisen, B. 1991: Linkage studies in autosomal recessive ichthyosis. Cytogenetics and Cell Genetics 58(1-4): 2112-2113
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Pras, E.; Arber, N.; Shapiro, J.; Aksentijevich, I.; Katz, G.; Harell, D.; Liberman, U.; Pras, M.; Kastner, D.L. 1994: Linkage studies in cystinuria. Journal of Cellular Biochemistry Suppl 1994(18 Part A): 208
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Richard, G.; Whyte, Y.M.; Smith, L.; Itin, P.; Hohl, D.; Wollina, U.; EpsteinE.Jr.; Lin, J.P.; Bale, S.J. 1996: Linkage studies in erythrokeratodermas Fine mapping, genetic heterogeneity, and analysis of candidate genes. American Journal of Human Genetics 59(4 Suppl): A233
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Hyden Granskog, C.; Salonen, R.; Von Koskull, H. 1991: Linkage studies in families with hereditary incontinentia pigmenti. American Journal of Human Genetics 49(4 Suppl): 344
Meera, K.P. 1992: Linkage studies in hereditary nonpolyposis colorectal cancer. Anticancer Research 12(6A): 1859
Compton, J.G.; Digiovanna, J.J.; Austin, F.; Peden, S.; Abangan, D.; Bale, S.J. 1997: Linkage studies in ichthyosis vulgaris. Journal of Investigative Dermatology 108(4): 646
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Carson W.J.; Maclead P.L.; Vincent D.; Nexarati M.; Radvany J.; Sequeiros J.; Coutinho P.; White B.; Forse R.A.; Et Al 1991: Linkage studies in machado joseph disease. American Journal of Human Genetics 49(4 Suppl): 337
Klintworth, G.K.; Vance, J.M.; Lennon, F.; Jonasson, F.; Wilkinson, K.M.; Pericak Vance, M.A. 1992: Linkage studies in macular corneal dystrophy. American Journal of Human Genetics 51(4 Suppl): A365
Speer M.C.; Pericak Vance M.A.; Yamaoka L.; Gilbert J.; Lee J.; Hung W Y.; Laberge C.; Thibault M.C.; Mathieu J.; Et Al 1989: Linkage studies in myotonic dystrophy. American Journal of Human Genetics 45(4 Suppl): A163
Roses, A.D.; Yamaoka, L.H.; Hung W Y.; Speer, M.C.; Laberge, C.; Thibault M C.; Mathieu, J.; Pericak Vance, M.A. 1989: Linkage studies in myotonic muscular dystrophy. Cytogenetics and Cell Genetics 51(1-4): 1069
Poyhonen, M.; Kytola, S.; Leisti, J. 1997: Linkage studies in neurofibromatosis-evidence of reduced penetrance of the NF1 gene?. American Journal of Human Genetics 61(4 Suppl): A402
Cooper, D.W.; Wilton, A.N.; Parsons, Y.M.; Brennecke, S.P. 1991: Linkage studies in pre eclampsia eclampsia pe e. American Journal of Human Genetics 49(4 Suppl): 214
Avramopoulos, D.; Kitsos, G.; Grigoriadou, M.; Economou Petersen, E.; Vassilopoulos, D.; Psilas, K.; Petersen, M.B. 1994: Linkage studies in primary open angle glaucoma. American Journal of Human Genetics 55(3 Suppl): A345
Lehesjoki A E.; Koskiniemi M.; Sistonen P.; Norio R.; De La Chapelle A. 1991: Linkage studies in progressive myoclonus epilepsy. American Journal of Human Genetics 49(4 Suppl): 16
Lehesjoki A E.; Koskiniemi M.; Sistonen P.; Norio R.; De La Chapelle A. 1991: Linkage studies in progressive myoclonus epilepsy of unverricht lundborg type epm1. Cytogenetics and Cell Genetics 58(1-4): 2037
Blanton, S.H.; Francomano, C.F.; Horton, W.A.; Wang, Y.; Conner, B.; Hecht, J.T. 1992: Linkage studies in pseudoachondroplasia. American Journal of Human Genetics 51(4 Suppl): A360
Faucher, M.C.; Vincent, D.; Carson, W.J.; Mathieu, J.; Prevost, C.; Bouchard, J.P.; Rouleau, G.A. 1991: Linkage studies in sensorimotor neuropathy with agenesis of corpus callosum. American Journal of Human Genetics 49(4 Suppl): 339
Byth, B.C.; Wells, R.A.; Daniels, R.J.; Hislop, J.; Thomas, N.; Dubowitz, V.; Gilliam, T.C.; Zerres, K.; Davies, K.E. 1989: Linkage studies in spinal muscular atrophy. Cytogenetics and Cell Genetics 51(1-4): 973-974
Lopes Cendes, I.; Andermann, E.; Gerstenbrand, F.; Bosch, S.; Wagner, M.; Andermann, F.; Donat, J.; Shokeir, M.; Rouleau, G. 1993: Linkage studies in spinocerebellar ataxia Evidence showing that the recently described SCA 2 locus is not a private gene. Neurology 43(4 Suppl 2): A359
Den Bieman, M.; Otsen, M.; Balling, R.; Jacob, H.J.; Hedrich, H.J.; Van Zutphen, L.F.M. 1994: Linkage studies in the laboratory rat Combined mapping of microsatellite, biochemical, immunological and RFLP markers. Animal Genetics 25(Suppl 2): 47
Stambolian, D.; Bond, A.; Lewis, R.A.; Buetow, K.H.; Nussbaum, R.L. 1989: Linkage studies in the nance horan syndrome using eight polymorphic dna probes from the short arm of x chromosome. Cytogenetics and Cell Genetics 51(1-4): 1085
Clark, R.F.; Martinez, A.; He, C.; Ruiz, A.; Kosik, K.; Lopera, F.; Behrens, I.M.; Busfield, F.; Madrigal, L.; Ossa, J.; Norton, J.; Goate, A.M.; Lendon, C.L. 1995: Linkage studies in three large early onset Alzheimers disease pedigrees from Colombia. American Journal of Human Genetics 57(4 Suppl): A189
Merkens, E.C.; Janssen, L.A.J.; Lindhout, D.; Hesseling Janssen, A.L.W.; Sandkuyl, L.A.; Sampson, J.R.; Halley, D.J.J. 1991: Linkage studies in tuberous sclerosis and their clinical relevance. American Journal of Human Genetics 49(4 Suppl): 342
Kandt, R.S.; Pericak-Vance, M.A.; Hung, W.Y.; Gardner, R.J.; Crossen, P.E.; Nellist, M.D.; Speer, M.C.; Roses, A.D. 1991: Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!. Annals of the new York Academy of Sciences 615: 284-297
Northrup, H.; Kwiatkowski, D.J.; Rodriguez, E.Jr; Roach, E.S.; Dobyns, W.B.; Lewis, R.A.; Blanton, S.H. 1991: Linkage studies in tuberous sclerosis using gt repeat polymorphisms. American Journal of Human Genetics 49(4 Suppl): 353
Gorski, S.M.; Adams, K.J.; Birch, P.H.; Chodirker, B.; Greenberg, C.R.; Goodfellow, P.J. 1992: Linkage studies in two families with X-linked cleft palate and ankyloglossia. American Journal of Human Genetics 51(4 Suppl): A188
Vance, J.M.; Small, K.; Stajich, J.; Jones, M.A.; Roses, A.D.; Pericak Vance, M.A. 1989: Linkage studies in von hippel lindau disease. Cytogenetics and Cell Genetics 51(1-4): 1097
Pericak Vance, M.A.; Vance, J.M.; Small, K.; Stajich, J.; Yamaoka, L.; Jones, M.A.; Roses, A.D. 1989: Linkage studies in von hippel lindau disease vhl. American Journal of Human Genetics 45(4 Suppl): A156
Nance, M.A.; Sane, K.S. 1991: Linkage studies in x linked gonadal dysgenesis. American Journal of Human Genetics 49(4 Suppl): 352
Van Schooneveld, M.; Hogenkamp, T.; Orth, U.; Neugebauer, M.; Lisch, K.; Bleeker Wagemakers, E.M.; Gal, A. 1989: Linkage studies in x linked juvenile retinoschisis. Cytogenetics and Cell Genetics 51(1-4): 1096
Graham, K.; Yee, R.; Barletta, J.; Mullen, L.; Small, K. 1995: Linkage studies of Reiss-Buckler corneal dystrophy. IOVS Investigative Ophthalmology and Visual Science 36(4): S144
Northrup, H.; RodriguezEstanislado, J.; Au, K.S.; Blanton, S.; Dobyns, W.B. 1997: Linkage studies of Walker-Warburg syndrome and chromosome 9q31-32. Annals of Human Genetics 61(3): 218-219
Gerhard, D.S.; Todd, R.D.; Van Eerdewegh, P.; Reich, T. 1992: Linkage studies of bipolar affective disorders in a large American pedigree. American Journal of Human Genetics 51(4 Suppl): A188
Dawson, E.; Parfitt, E.; Roberts, Q.; Daniels, J.; Lim, L.; Sham, P.; Nöthen, M.; Propping, P.; Lanczik, M.; Maier, W. 1995: Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. American Journal of Medical Genetics 60(2): 94-102
Craddock, N.; Bowen, T.; Kirov, G.; Gill, M.; Spurlock, G.; Vallada, H.; Powell, J.; Murray, R.; Mcguffin, P.; Collier, D.; Owen, M.J. 1996: Linkage studies of bipolar disorder with chromosome 18 markers. American Journal of Human Genetics 59(4 Suppl): A381
Berrettina, W.H.; Detera Wadleigh, S.D.; Goldin, L.R.; Martinez, M.; Hsieh W T.; Hoehe, M.; Robb, A.S.; Gershon, E.S. 1991: Linkage studies of bipolar illness. American Journal of Human Genetics 49(4 Suppl): 336
Rubin, L.R.; Amos, C.I.; Falk Wade, J.; Martin, J.; Bonney, G.E.; Bale, S.J.; Gladman, D.; Siminovitch, K.; Little, H.; Rubinstein, J. 1992: Linkage studies of class I MHC region genes in ankylosing spondylitis. American Journal of Human Genetics 51(4 Suppl): A34
Mathews, K.D.; Bailey, H.L.; Mills, K.A.; Schutte, B.C.; Murray, J.C. 1992: Linkage studies of facioscapulohumeral dystrophy. American Journal of Human Genetics 51(4 Suppl): A195
Spurr, N.; Adams, M.; Kelsell, D.; Murday, V.A.; Solomon, E.; Turner, G.; Williams, M.A.T.; Bishop, D.T. 1991: Linkage studies of familial breast cancer evidence for 17q linkage. American Journal of Human Genetics 49(4 Suppl): 360
Donald, J.A.; Barendse, W.; Cooper, D.W. 1989: Linkage studies of HLA and insulin gene restriction fragment length polymorphisms in families with IDDM. Genetic Epidemiology 6(1): 77-81
Liu, A.W.; Weissbecker, K.A.; Delgado Escueta, A.; Serratosa, J.M.; Treiman, L.; Sparkes, R.; Park, M.S. 1991: Linkage studies of juvenile myoclonic epilepsy. Cytogenetics and Cell Genetics 58(1-4): 1913-1914
Bruni A.C.; Montesi M.P.; Manfredi R.; Di Cello A.; Gei G.; Fragiacomo D.; De Fazio P.; Puca M.; Amati A.; Foncin J.F. 1992: Linkage studies of major affective disorders the impact of the extension of pedigrees. European Psychiatry 7(3): 145-146
Kimberling, W.J.; Pieke, S.A.; Gabow, P. 1989: Linkage studies of polycystic kidney disease type 2. American Journal of Human Genetics 45(4 Suppl): A50
Diehl, S.; Marazita, M.L.; Bodurtha, J.; Spence, J.E.; Shaver Arnos, K.; Allen, T.; Rawlings, B.; Nance, W.E. 1989: Linkage studies of profound prelingual deafness. Cytogenetics and Cell Genetics 51(1-4): 989
Su Y.; Bray J.; Burke J.; Inomata T.; Maclean C.; Marazita M.; Murphy B.; Nie L.; Nuallain M.N.; Et Al 1991: Linkage studies of schizophrenia exclusion of candidate regions on chromosomes 5q and 11q. American Journal of Human Genetics 49(4 Suppl): 361
Su Y.; Maclean C.J.; Walsh D.; O'hare A.; Mcguire M.; Kidd K.K.; Diehl S.R.; Kendler K.S. 1989: Linkage studies of schizophrenia in irish pedigrees. Cytogenetics and Cell Genetics 51(1-4): 989
Diehl S.R.; Su Y.; Maclean C.J.; Walsh D.; O'hare A.; Mcguire M.; Kendler K.S. 1989: Linkage studies of schizophrenia using polymorphic dna markers. Behavior Genetics 19(6): 753
Owen, M.; Parfitt, E.; Sargeant, M.; Asherson, P.; Mcguffin, P.; Taylor, C.; Collier, D.; Powell, J.; Murray, R.; Gill, M. 1991: Linkage studies of schizophrenia with markers of chromosome 11q. American Journal of Human Genetics 49(4 Suppl): 354
D.L.P.z, M.A.; Haines, J.L.; Heinis, R.; Agarwal, R.; Lennon, F.; Pericak Vance, M.A. 1997: Linkage studies of the Malattia Leventinese locus to age-related macular degeneration. American Journal of Human Genetics 61(4 Suppl): A273
Riley, B.P.; Tahir, E.; Rajagopalan, S.; Mogudi Carter, M.; Jenkins, T.; Williamson, R. 1996: Linkage studies of the N-methyl-D-aspartate receptor subunit gene regions and schizophrenia in southern African Bantu-speaking families. American Journal of Human Genetics 59(4 Suppl): A387
Northrup, H.; Roach, E.S.; Lewis, R.A.; RodriguezE.Jr; Dobyns, W.B.; Reeders, S.T.; Blanton, S.H. 1992: Linkage studies of tuberous sclerosis complex to markers on chromosome 16p133. American Journal of Human Genetics 51(4 Suppl): A197
Gorski, S.M.; Adams, K.J.; Birch, P.H.; Friedman, J.M.; Goodfellow, P.J. 1991: Linkage studies of x linked cleft palate in a british columbia native kindred. American Journal of Human Genetics 49(4 Suppl): 341
Heinzmann, C.; Kojis, T.L.; Flodman, P.; Mullen, M.L.; Gonzalez, P.; ZiglerJ.S.Jr.; Spence, M.A.; Bateman, J.B. 1994: Linkage studies of zeta crystallin with human autosomal domain congenital cataracts. IOVS Investigative Ophthalmology and Visual Science 35(4): 2115
Vallada, H.P.; Gill, M.; Sham, P.; Lim, L.C.; Nanko, S.; Asherson, P.; Murray, R.M.; McGuffin, P.; Owen, M.; Collier, D. 1995: Linkage studies on chromosome 22 in familial schizophrenia. American Journal of Medical Genetics 60(2): 139-146
Khan P.M.; Tops C.M.J.; Breukel C.; Wijnen J.T.; V.D.Klift H.M.; Van Leeuwen Cornelisse I.S.J.; Vasen H.F.A.; Griffioen G.; Den Hartog Jager F.C.A.; Lamers C.B.H.W. 1990: Linkage studies on familial adenomatous polyposis fap in the netherlands. International Journal of Colorectal Disease 5(1): 56-57
Newton, R.; Jensson, O.; Arnason, A.; Henderson, D.; Moore, G. 1989: Linkage studies on families showing a rare form of spina bifida. Journal of Cellular Biochemistry Suppl (13 Part D): 24
Griffiths, L.R.; Zwi, M.B.; Mcleod, J.G.; Nicholson, G.A. 1990: Linkage studies on hypertrophic motor and sensory neuropathy type i. Lovelace, R E And H K Shapiro (Ed ) Neurology And Neurobiology, Vol 53 Charcot-Marie-Tooth Disorders: Pathophysiology, Molecular Genetics, And Therapy; Second International Conference, Harriman, New York, Usa, June 28-July 1, 1987 Xxvii+448p Wiley-Liss: New York, New York, Usa Illus 269-278
Yuzbasiyan Gurkan, V.; Wagnitz, S.; Blanton, S.H.; Brewer, G.J. 1991: Linkage studies on inherited canine copper toxicosis. American Journal of Human Genetics 49(4 Suppl): 334
Fujikawa, K.; Kawaguchi, Y.; Doira, H.; Banno, Y.; Koga, K. 1996: Linkage studies on the scanty vitellin egg mutant of Bombyx mori. Journal of Sericultural Science of Japan 65(2): 145-146
Eiberg, H.; Marner, E.; Rosenberg, T.; Mohr, J. 1989: Linkage studies using protein enzyme and blood group markers marners cataract zonular linked to haptoglobin on chromosome 16. Clinical Genetics 35(3): 214
Ross, D.A.; Zwi, M.; Block, J.; Mcleod, J.G.; Nicholson, G.A. 1989: Linkage studies with friedreichs ataxia in australian pedigrees. Cytogenetics and Cell Genetics 51(1-4): 1069
Hall, F.C.; Walsh, S.; Nicod, A.; Butcher, S.; Wordsworth, B.P.; Hardwick, L.J. 1996: Linkage study across the TCRA and TCRB loci in multiplex families with rheumatoid arthritis. Arthritis and Rheumatism 39(9 Suppl): S60
Fang B.; Wang M.; Huang S.; Li J.; Ye L.; Gao X.; Tang X.; Luo W.H.Y. 1991: Linkage study and presymptomatic diagnosis of wilson disease in chinese. American Journal of Human Genetics 49(4 Suppl): 186
Chiarella, J.; Goldberg, A.C.; Abel, L.; Kalil, J.; Dessein, A. 1996: Linkage study between HLA antigens and a major gene involved in susceptibility/resistance to infection to Schistosoma mansoni. Human Immunology 47(1-2): 124
Chiarella, J.; Goldberg, A.C.; Abel, L.; Kalil, J.; Dessein, A. 1995: Linkage study between a schistosomiasis susceptibility gene and HLA in families from a Brazilian endemic area. 9TH INTERNATIONAL CONGRESS OF IMMUNOLOGY Author The 9th International Congress of Immunology : 560
De Michele, G.; Marconi, R.; Cavalcanti, F.; Casari, G.; De Fusco, M.; Mandato, C.; Filla, A.; Campanella, G.; Cocozza, S. 1997: Linkage study in an Italian family with autosomal recessive spastic paraplegia. Journal of the Neurological Sciences 150(Suppl ): S41
Ozen, S.; Akarsu, A.N.; Saatci, U.; Bakkaloglu, A.; Sarfarazi, M. 1996: Linkage study of Turkish familial mediterranean fever to 16p133 and evidence for genetic heterogeneity. American Journal of Human Genetics 59(4 Suppl): A231
Barr, C.L.; Kennedy, J.L.; Pakstis, A.J.; Castiglione, C.M.; Kidd, J.R.; Wetterberg, L.; Kidd, K.K. 1994: Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region. Schizophrenia Bulletin 20(2): 277-286
Nomura, S.; Fukushima, T.; Daly, M.J.; Naito, I.; Tokura, T.; Chihara, J.; Takebayashi, S.; Fujieda, M.; Sasaki, T.; Osawa, G. 1997: Linkage study of autosomal alport syndrome. Journal of the American Society of Nephrology 9(Program and Abstr. Issue): 394A
Fossdal, R.; Asmundsson, P.; Bodvarsson, M.; Jensson, O. 1991: Linkage study of autosomal dominant polycystic kidney disease in iceland. American Journal of Human Genetics 49(4 Suppl): 340
Brett, P.M.; Yiannakou, J.Y.; Curtis, D.; Mathew, C.G.; Rosen Bronson, S.; Ciclitira, P.J. 1997: Linkage study of chromosome 21 and the downs dependent region in the genetic aetiology of Celiac Disease. Gastroenterology 112(4 Suppl): A350
Simard, L.R.; Rochette, C.; Morgan, K.; Vanasse, M.; Melancon, S.B.; Labuda, D. 1991: Linkage study of chronic spinal muscular atrophy sma confirmation of close linkage to d5s39 in french canadian families. American Journal of Human Genetics 49(4 Suppl): 359
Eiberg, H.; Mohr, J.; Bisgaard, M.L.; Shen, L. 1991: Linkage study of complement c6 on chromosome 5. Cytogenetics and Cell Genetics 58(1-4): 1895
Wakisaka, A.; Sasaki, H.; Katoh, T.; Yoshida, M.C.; Hamada, T.; Shima, K.; Matsuura, T.; Takenouchi, T.; Tashiro, K. 1989: Linkage study of dominantly inherited spinocerebellar degeneration. Cytogenetics and Cell Genetics 51(1-4): 1101
Glass, I.A.; White, E.M.; Pirrit, L.A.; Bell, M.V.; Connor, J.M. 1990: Linkage study of f8 in the fragile x syndrome. Journal of Medical Genetics 27(3): 208
Shugart, Y.; Chatkupt, S.; Horan, J.T.; Dermody, J.J.; Koenigsberger, M.R.; Mariman, E.C.M.; Hamel, B.C.J.; Hol, F.A.; Geurdis, M.P.A. 1993: Linkage study of familial myelomeningocele and a candidate region. Neurology 43(4 Suppl 2): A285
Best, L.G.; North, K.E.; Li, X.; Palmieri, V.; Umans, J.G.; MacCluer, J.; Laston, S.; Haack, K.; Goring, H.; Diego, V.P.; Almasy, L.; Lee, E.T.; Tracy, R.P.; Cole, S. 2008: Linkage study of fibrinogen levels: the Strong Heart Family Study. Bmc Medical Genetics 9: 77
Blanton, S.H.; Hogue, D.; Wells, D.E.; Wagner, M.J.; Hecht, J.T. 1994: Linkage study of hereditary multiple exostosis. American Journal of Human Genetics 55(3 Suppl): A180
Stein, J.D.; Nelson, L.D.; Conner, B.J.; Weber, J.L.; Malcolm, S.; Gasser, D.L.; Blanton, S.H.; Hecht, J.T. 1994: Linkage study of nonsyndromic cleft lip with or without cleft palate using candidate genes and mapped polymorphic markers. American Journal of Human Genetics 55(3 Suppl): A354
Vieland, V.J.; Knowles, J.A.; Fyer, A.J.; Stefanovich, M.; Freimer, N.F.; Lish, J.; Adams, P.; Woodley, K.; Rassnick, H.; Heiman, G.A.; White, P.; Das, K.; Klein, D.F.; Ott, J.; Weissman, M.M.; Gilliam, T.C.nrad 1994: Linkage study of panic disorder A preliminary report. Gershon, E S , Cloninger, C R American Psychopathological Association Series; Genetic approaches to mental disorders 345-354
Fryburg, J.S.; Bale, S.J.; Mcbride, O.W.; Mulvihill, J.J.; Bale, A.E. 1989: Linkage study of the nevoid basal cell carcinoma syndrome nbccs. Cytogenetics and Cell Genetics 51(1-4): 1000
Ge, P.; Mitsuishi, Y.; Bibee, K.I.; Terasaki, P.I. 1997: Linkage study of the polymorphism of HLA-B and MICA. Human Immunology 55(Suppl 1): 113
Di Cera, E. 1994: Linkage thermodynamics. Methods in Enzymology 232: 655-683
D.Cera, E. 1992: Linkage thermodynamics of thrombin function. Biophysical Journal 61(2 Part 2): A413