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Section 43

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References:

Littlefield, L.G.; Colyer, S.P.; Joiner, E.E.; DuFrain, R.J.; Frome, E.; Cohen, M.M. 1981: Chromosomal radiation sensitivity in ataxia telangiectasia long-term lymphoblastoid cell lines. Cytogenetics and Cell Genetics 31(4): 203-213
Sasaki, M.S.; Tonomura, A. 1969: Chromosomal radiosensitivity in Down's syndrome. Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 14(2): 81-92
Parshad, R.; Gantt, R.; Sanford, K.K.; Jones, G.M. 1984: Chromosomal radiosensitivity of human tumor cells during the G2 cell cycle period. Cancer Research 44(12 Part 1): 5577-5582
Sevan'kaev, A.V.; Nasonova, V.A.; Golovinova, G.I. 1983: Chromosomal reaction of human lymphocytes to fractionated neutron doses in in vitro irradiation. Radiobiologiia 23(3): 332-336
Adair, G.M.; Stallings, R.L.; Siciliano, M.J. 1984: Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7. Somatic Cell and Molecular Genetics 10(3): 283-295
Smithies, O. 1965: Chromosomal rearrangements and protein structure. Bibliotheca Haematologica 23: 373-374
Martin, P.A.; Thorburn, M.J.; Smith-Read, E.H. 1970: Chromosomal rearrangements in three generations of a Jamaican family. A possible further example of recombinational imbalance. Cytogenetics 9(5): 360-368
Toussaint, A.; Faelen, M.; Résibois, A. 1981: Chromosomal rearrangements induced by mini-Mu and mini-D108: mini review and new data. Gene 14(1-2): 115-119
Faelen, M.; Toussaint, A. 1980: Chromosomal rearrangements induced by temperate bacteriophage D108. Journal of Bacteriology 143(2): 1029-1030
Fleischman, E.W.; Prigogina, E.L.; Iljinskaja, G.W.; Konstantinova, L.N.; Puchkova, G.P.; Volkova, M.A.; Frenkel, M.A.; Balakirev, S.A. 1983: Chromosomal rearrangements with a common breakpoint at 6p23 in five cases of myeloid leukemia. Human Genetics 64(3): 254-256
Haussler, M.R.; Norman, A.W. 1969: Chromosomal receptor for a vitamin D metabolite. Proceedings of the National Academy of Sciences of the United States of America 62(1): 155-162
Wang, N.; Trend, B.; Kaung, H.L.; Wang, T. 1982: Chromosomal replication asynchrony of a human breast carcinoma cell line. I. studied by continuous BrdU incorporation and G-banding analysis. Cancer Genetics and Cytogenetics 7(2): 173-180
Zyskind, J.W.; Cleary, J.M.; Brusilow, W.S.; Harding, N.E.; Smith, D.W. 1983: Chromosomal replication origin from the marine bacterium Vibrio harveyi functions in Escherichia coli: oriC consensus sequence. Proceedings of the National Academy of Sciences of the United States of America 80(5): 1164-1168
Chiampo, L.; Gallinaro, P. 1967: Chromosomal research in Peutz-Jeghers familial disease. Bollettino della Societa Italiana di Biologia Sperimentale 43(19): 1303-1305
Sannoe, Y.; Kimura, N. 1966: Chromosomal response of cancer cells to antineoplastic agents. Gan no Rinsho. Japan Journal of Cancer Clinics 12(2): 89-100
Dahmus, M.E.; McConnell, D.J. 1969: Chromosomal ribonucleic acid of rat ascites cells. Biochemistry 8(4): 1524-1534
Mellman, W.J. 1974: Chromosomal screening of human populations; a bioethical prospectus. Birth Defects Original Article Series 10(6): 123-136
Berger, A.; Simma, W.; Fischer, P. 1972: Chromosomal sex determination in idiopathic gynaecomastia. Wiener Klinische Wochenschrift 84(42): 699-701
Guinet, P.; Laurent, C.; Putelat, R.; Bansilion, V.; Vallon, C. 1965: Chromosomal sex in true hermaphrodism. La Revue Lyonnaise de Medecine 14(17): 27-52
Parker, D.L.; Glaser, D.A. 1974: Chromosomal sites of DNA-membrane attachment in Escherichia coli. Journal of Molecular Biology 87(2): 153-168
Rabin, M.; Uhlenbeck, O.C.; Steffensen, D.M.; Mangel, W.F. 1984: Chromosomal sites of integration of simian virus 40 DNA sequences mapped by in situ hybridization in two transformed hybrid cell lines. Journal of Virology 49(2): 445-451
Sultan, K.M.; Munné, S.; Palermo, G.D.; Alikani, M.; Cohen, J. 1995: Chromosomal status of uni-pronuclear human zygotes following in-vitro fertilization and intracytoplasmic sperm injection. Human Reproduction 10(1): 132-136
Jones, J.D.; Flavell, R.B. 1983: Chromosomal structure and arrangement of repeated DNA sequences in the telomeric heterochromatin of Secale cereale and its relatives. Cold Spring Harbor Symposia on Quantitative Biology 47 Pt 2: 1209-1213
Minghetti, P.P.; Harper, M.E.; Alpert, E.; Dugaiczyk, A. 1983: Chromosomal structure and localization of the human alpha-fetoprotein gene. Annals of the new York Academy of Sciences 417: 1-12
Orlov, V.N.; Kozlovskiĭ, A.I. 1969: Chromosomal structure of 2 geographically removed populations and their place in the general system of chromosomal polymorphism in the common shrew. Tsitologiia 11(9): 1129-1136
Szczepski, O.; Korbas, J.; Bialecki, M. 1970: Chromosomal studies and sex determination in children. Pediatria Polska 45(9): 1033-1040
De Grouchy, J.; Billardon, C.; Roubin, M. 1970: Chromosomal studies from cell cultures. Technical modifications. Annales de Genetique 13(2): 141-143
Philippe, N.; Requin, C.; Germain, D. 1971: Chromosomal studies in 6 cases of Blackfan-Diamond anemia. Pediatrie 26(1): 47-54
Chun, T.; Alexander, D.S.; Bryans, A.M.; Haust, M.D. 1966: Chromosomal studies in children with mumps, chickenpox, measles and measles vaccination. Canadian Medical Association Journal 94(3): 126-129
Wolf, U.; Merker, H.; Böckelmann, W. 1966: Chromosomal studies in chronic myeloic leukemia. Klinische Wochenschrift 44(1): 12-19
Andreesu, M.; Matefsu, C.; Mogos, I.; Mudric, V. 1974: Chromosomal studies in correlation with other biologic constants in neoplasms treated by chemotherapy. Minerva Medica 65(34): 1863-1872
Ahrens, K. 1967: Chromosomal studies in craniofacial abnormalities. Hno 15(4): 106-109
Castoldi, G.; Mitus, W.J.; Yam, L.T.; Crosby, W.H. 1968: Chromosomal studies in erythroleukemia and chronic erythremic myelosis. Blood 31(2): 202-215
Herrmann, R.P.; Chipper, L.; Bell, S. 1982: Chromosomal studies in healthy blood donors with IgA deficiency. Clinical Genetics 22(5): 231-233
Moreno, R.; Curotto, B.; Seebach, C.; Lacassie, Y. 1982: Chromosomal studies in infants with severe protein-calorie malnutrition. Revista Chilena de Pediatria 53(5): 416-418
Dambska, J. 1969: Chromosomal studies in malignant lymphogranulomatosis. Polskie Archiwum Medycyny Wewnetrznej 43(2): 1107-1113
Franke, F.; Lampert, F. 1982: Chromosomal studies in metastatic neuroblastoma. Onkologie 5(6): 268-272
Brown, R.K.; Smith, W.L. 1964: Chromosomal studies in ovarian dysgenesis. Transactions of the new England Obstetrical and Gynecological Society 18: 47-54
Stevenson, A.C.; Bedford, J.; Hill, A.G.; Hill, H.F. 1971: Chromosomal studies in patients taking phenylbutazone. Annals of the Rheumatic Diseases 30(5): 487-500
Przeździak, B.; Szczerkowska, Z. 1970: Chromosomal studies in patients with a cleft palate. Wiadomosci Lekarskie 23(22): 1963-1965
Eberle, P.; Klostermann, G.F. 1968: Chromosomal studies in peutz-touraine-jeghers-syndrome. Archiv für Klinische und Experimentelle Dermatologie 231(4): 437-449
Lejeune, J. 1966: Chromosomal studies in psychiatry. Recent Advances in Biological Psychiatry 9: 13-20
Adler, P.; Gierke, L.W. 1971: Chromosomal studies in relation to abortion. Journal of the American Osteopathic Association 70(12): 1319-1323
Serr, D.M.; Padeh, B.; Mashiach, S.; Shaki, R. 1969: Chromosomal studies in tumors of embryonic origin. Obstetrics and Gynecology 33(3): 324-332
Stevenson, A.C.; Clarke, G.; Patel, C.R.; Hughes, D.T. 1973: Chromosomal studies in vivo and in vitro of trimethoprim and sulphamethoxazole (co-trimoxazole). Mutation Research 17(2): 255-260
Kulkarni, P.S.; Mondkar, V.P.; Sonawalla, A.B.; Ambani, L.M. 1984: Chromosomal studies of peripheral blood from epileptic patients treated with phenobarbital and/or diphenylhydantoin. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association 22(12): 1009-1012
Joneja, M.G.; Travill, A.A.; Scott, G.D. 1972: Chromosomal studies of prison inmates with relationship to offence characteristics. Canadian Psychiatric Association Journal 17(2): 147-148
Egozcue, J. 1972: Chromosomal studies of selected cells: the V-cell of Rauscher's murine leukemia. Annales de Genetique 15(1): 25-28
Kawasaki, M. 1968: Chromosomal studies of trophoblastic tumor. Nihon Sanka Fujinka Gakkai Zasshi 20(7): 699-707
Hughes, D.T.; Cavanagh, N. 1983: Chromosomal studies on children with phocomelia, exposed to debendox during early pregnancy. Lancet 2(8346): 399
Ijiri, K. 1983: Chromosomal studies on radiation-induced gynogenesis and diploid gynogenesis in the fish Oryzias latipes. Journal of Radiation Research 24(2): 184-195
Emoto, H. 1967: Chromosomal studies on xenogeneic transplantation of virus-induced tumor. Journal of Osaka University Dental School 12(1): 127-138
Ujházy, V. 1968: Chromosomal studies with the nitrogen mustard-sensitive and resistant Yoshida tumour. Neoplasma 15(6): 657-661
Tsunotani, T. 1970: Chromosomal study in gyneco-obstetrical field. Chromosomal study of sterility and congenital anomalies. Nihon Sanka Fujinka Gakkai Zasshi 22(8): 833-842
Ichinoe, K.; Fukushima, T.; Nishitani, I.; Fujisawa, M.; Araya, T. 1970: Chromosomal study in gynecolo-obstetrical field. Chromosomes in tumors. Nihon Sanka Fujinka Gakkai Zasshi 22(8): 843-852
Cada, K.; Soudek, D. 1968: Chromosomal study in otosclerosis and in van der Hoeve de Kleyn's syndrome. Ceskoslovenska Otolaryngologie 17(5): 285-287
Cendrowski, W.; Zajaczkowska, K. 1970: Chromosomal study in patients with multiple sclerosis. Neurologia i Neurochirurgia Polska 4(1): 69-70
Rousseau, M.F. 1973: Chromosomal study of 20 embryonic tumors after short term culture. Biomedicine / 19(6): 275-280
Ortega Aramburu, J.J.; García-San Miguel, J. 1972: Chromosomal study of Fanconi's aplastic anemia. Apropos of 2 cases. Sangre 17(1): 87-100
Baserga, A.; Castoldi, G.L.; Franceschini, F. 1966: Chromosomal study of chronic lymphocytic leukemia. Schweizerische Medizinische Wochenschrift 96(37): 1220-1222
Saint-Aubert, P.; Maillard, E.; Walbaum, R.; Delmas-Marsalet, Y.; Deminatti, M.; Fontaine, G. 1968: Chromosomal study of human hermaphroditism. Apropos of a case with 46,XY 46,-XX karyotpe. Annales de Pediatrie 15(1): 18-26
Berger, R.; Lacour, J. 1973: Chromosomal study of malignant melanomas. Biomedicine / 19(1): 22-27
Iartseva, N.M.; Kotsiubinskiĭ, N.N.; Mamaeva, S.E. 1984: Chromosomal study of polycythemia during different stages of the disease. Tsitologiia 26(3): 323-329
Battaglia, E.; Guanti, G.; Barsanti, P.; Petrinelli, P. 1971: Chromosomal survey in 298 normal subjects and 1,253 cases of congenital disorders during 1966-1970. Acta Geneticae Medicae et Gemellologiae 20(2): 123-173
Osowiecki, H. 1974: Chromosomal theory of heredity. Pielegniarka i Polozna 12: 5-6
Clowes, R.C.; Moody, E.E. 1966: Chromosomal transfer from "recombination-deficient" strains of Escherichia coli K-12. Genetics 53(4): 717-726
Cooke, M.; Meynell, E. 1969: Chromosomal transfer mediated by de-repressed R factors in F- Escherichia coli K12. Genetical Research 14(1): 79-87
Turc-Carel, C.; Philip, I.; Berger, M.P.; Philip, T.; Lenoir, G. 1983: Chromosomal translocation (11; 22) in cell lines of Ewing's sarcoma. Comptes Rendus des Seances de l'Academie des Sciences. Serie Iii Sciences de la Vie 296(23): 1101-1103
Dillman, R.O. 1984: Chromosomal translocation in a child with chronic lymphocytic leukemia. New England Journal of Medicine 310(7): 469
Sonnier, J.A.; Buchanan, G.R.; Howard-Peebles, P.N.; Rutledge, J.; Smith, R.G. 1983: Chromosomal translocation involving the immunoglobulin kappa-chain and heavy-chain loci in a child with chronic lymphocytic leukemia. New England Journal of Medicine 309(10): 590-594
Ohno, S.; Migita, S.; Wiener, F.; Babonits, M.; Klein, G.; Mushinski, J.F.; Potter, M. 1984: Chromosomal translocations activating myc sequences and transduction of v-abl are critical events in the rapid induction of plasmacytomas by pristane and abelson virus. Journal of Experimental Medicine 159(6): 1762-1777
Murphy, S.B.; Harris, A.; Williams, D.L. 1984: Chromosomal translocations and timing of malignant transformation in Burkitt's lymphoma. New England Journal of Medicine 311(3): 195-196
Mark-Vendel, E.; Philip, T.; Ladjaj, Y.; Aboulola, M.; Lenoir, G.M. 1983: Chromosomal translocations in Algerian Burkitt's lymphoma. Lancet 2(8353): 788
Anonymous 1983: Chromosomal translocations in Ewing's sarcoma. New England Journal of Medicine 309(8): 496-498
Bernard, R.; Stahl, A.; Coignet, J.; Giraud, F.; Hartung, M.; Brusquet, Y.; Passeron, P. 1967: Chromosomal triploidy in a new-born infant with multiple malformations. Annales de Genetique 10(2): 70-74
Labiszewska-Jaruzelska, F.; Pisulska-Otremba, A.; Dziekanowska, D.; Dziuba, P.; Bulsiewicz, H.; Osuch-Jaczewska, R. 1972: Chromosomal trisomy of group D (Patau syndrome). Czasopismo Stomatologiczne 25(9): 865-867
Pogosiants, E.E. 1973: Chromosomal variability and carcinogenesis. Vestnik Akademii Meditsinskikh Nauk SSSR 28(1): 49-54
Ikeuchi, T.; Minowada, J.; Sandberg, A.A. 1971: Chromosomal variability in ten cloned sublines of a newly established Burkitt's lymphoma cell line. Cancer 28(2): 499-512
Taylor, M.B. 1970: Chromosomal variability in the D1 trisomy syndrome. West Virginia Medical Journal 66(3): 76
Taylor, M.B.; Juberg, R.C.; Jones, B.; Johnson, W.A. 1970: Chromosomal variability in the D1 trisomy syndrome. Three cases and review of the literature. American Journal of Diseases of Children 120(4): 374-381
Balzan, S.; Ronchi, V.N. 1981: Chromosomal variability of 2 species of Nicotiana in fluid culture. Bollettino della Societa Italiana di Biologia Sperimentale 57(15): 1596-1600
Kamenev, L.; Frederic, J.; André, A. 1983: Chromosomal variants in paternity research. Acta Medicinae Legalis et Socialis 33(2): 1163-1168
Terzi, M. 1974: Chromosomal variation and the origin of drug-resistant mutants in mammalian cell lines. Proceedings of the National Academy of Sciences of the United States of America 71(12): 5027-5031
Baker, R.J.; Lopez, G. 1970: Chromosomal variation in bats of the genus Uroderma (Phyllostomatidae). Journal of Mammalogy 51(4): 786-789
Eberle, P. 1970: Chromosomal viewpoints in the selection of experimental subjects. I. Medizinische Monatsschrift 24(8): 341-6 contd
Bender, W.; Spierer, P.; Hogness, D.S. 1983: Chromosomal walking and jumping to isolate DNA from the Ace and rosy loci and the bithorax complex in Drosophila melanogaster. Journal of Molecular Biology 168(1): 17-33
Spira, J.; Asjö, B.; Cochran, A.; Shen, F.W.; Wiener, F.; Klein, G. 1981: Chromosomal, histopathological and cell surface marker studies on Moloney virus induced lymphomas. Leukemia Research 5(2): 113-121
Alimena, G.; Dallapiccola, B.; Gastaldi, R.; Mandelli, F.; Brandt, L.; Mitelman, F.; Nilsson, P.G. 1982: Chromosomal, morphological and clinical correlations in blastic crisis of chronic myeloid leukaemia: a study of 69 cases. Scandinavian Journal of Haematology 28(2): 103-117
Paunow, S.; Laussmann, D. 1980: Chromosomal-bone-marrow changes after 137Cs incorporation in Dsungaric hamsters. Radiobiologia Radiotherapia 21(1): 30-35
Stuy, J.H. 1980: Chromosomally integrated conjugative plasmids are common in antibiotic-resistant Haemophilus influenzae. Journal of Bacteriology 142(3): 925-930
Nishino, H. 1984: Allotransplantation of isolated pancreatic islets in diabetic rats. Effect of culture on islet rejection. Nihon Geka Gakkai Zasshi 85(1): 38-48
Manolov, G.; Manolova, Y.; Klein, G.; Levan, A.; Kieler, J. 1981: Chromosome #14 markers in two Epstein-Barr virus (EBV)-transformed lymphoblastoid cell lines of normal origin differ from the Burkitt lymphoma (BL)-associated 14q+ marker. Cancer Genetics and Cytogenetics 4(2): 179-184
Atkin, N.B.; Brito-Babapulle, V. 1983: Chromosome 1 C-band heteromorphisms in patients with carcinoma in situ and invasive carcinoma of the cervix uteri. Australian and New Zealand Journal of Obstetrics and Gynaecology 23(2): 73-76
Desangles, F.; Saliou, P.; Antoine, H.M.; Laurens, A. 1984: Chromosome 11 abnormality in a case of acute monocytic leukemia (M5b). Annales de Medecine Interne 135(1): 51-53
Pueschel, S.M.; Padre-Mendoza, T. 1984: Chromosome 11 and Beckwith-Wiedemann syndrome. Journal of Pediatrics 104(3): 484-485
Gregoire, M.J.; Pernot, C.; Himont, F.; Pierson, M.; Gilgenkrantz, S. 1983: Chromosome 11 and cancer. Journal de Genetique Humaine 31(1): 31-36
Lungarotti, M.S.; Mariotti, G.; Quarta, C.; Delogu, A.; Fiore, C. 1980: Chromosome 13 deletion syndrome: report of a new case and discussion of the different etiologic patterns of retinoblastoma. Ophthalmologica. Journal International d'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift für Augenheilkunde 181(5): 245-250
Miyamoto, K.; Miyano, K.; Miyoshi, I.; Hamasaki, K.; Nishihara, R.; Terao, S.; Kimura, I.; Maeda, K.; Matsumura, K.; Nishijima, K.; Tanaka, T. 1980: Chromosome 14q+ in a Japanese patient with Burkitt's lymphoma. Acta Medica Okayama 34(1): 61-65
Miyoshi, I.; Miyamoto, K.; Sumida, M.; Nishihara, R.; Lai, M.; Yoshimoto, S.; Sato, J.; Kimura, I. 1981: Chromosome 14q+ in adult T-cell leukemia. Cancer Genetics and Cytogenetics 3(3): 251-259
Ledbetter, D.H.; Mascarello, J.T.; Riccardi, V.M.; Harper, V.D.; Airhart, S.D.; Strobel, R.J. 1982: Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases. American Journal of Human Genetics 34(2): 278-285
Kelly, S.; Almy, R.; Dagle, A. 1969: Chromosome 15 abnormality in a mentally retarded adult. Journal of Medical Genetics 6(4): 438-441
Mattei, M.G.; Souiah, N.; Mattei, J.F. 1984: Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis. Human Genetics 66(4): 313-334
Zhuang, J.; Hu, X.; Zhang, B. 1994: Chromosome 15 satellite enlargement and hereditary deafness. Zhonghua Er Bi Yan Hou Ke Za Zhi 29(4): 225-227
Wiener, F.; Babonits, M.; Spira, J.; Bregula, U.; Klein, G.; Merwin, R.M.; Asofsky, R.; Lynes, M.; Haughton, G. 1981: Chromosome 15 trisomy in spontaneous and carcinogen-induced murine lymphomas of B-cell origin. International Journal of Cancer 27(1): 51-58
de la Chapelle, A.; Lahtinen, R. 1983: Chromosome 16 and bone-marrow eosinophilia. New England Journal of Medicine 309(22): 1394
Kelly, S.; Almy, R. 1971: Chromosome 16 heterology. Nonspecific variation in karyotype?. New York State Journal of Medicine 71(19): 2297-2299
Testa, J.R.; Hogge, D.E.; Misawa, S.; Zandparsa, N. 1984: Chromosome 16 rearrangements in acute myelomonocytic leukemia with abnormal eosinophils. New England Journal of Medicine 310(7): 468-469
Takanishi, D.M.; Angriman, I.; Yaremko, M.L.; Montag, A.; Westbrook, C.A.; Michelassi, F. 1995: Chromosome 17p allelic loss in colorectal carcinoma. Clinical significance. Archives of Surgery 130(6): 585-588; Discussion: 588-589
Jacobsen, P.; Mikkelsen, M. 1968: Chromosome 18 abnormalities in a family with a translocation t(18p--, 21p+). Journal of Mental Deficiency Research 12(2): 144-161
Le Marec, B.; Lessard, M.; Renault, A.; Coutel, Y. 1971: Chromosome 18 long arm deletion. a case with unusual dermatoglyphics. Pediatrie 26(7): 749-757
García Báez, M.; Gonzälez Espinosa, C.; Serna Alonso, E.; Mota Moraleda, D. 1980: Chromosome 18 long-arm deletion. Report of 1 case. Anales Espanoles de Pediatria 13(11): 1001-1006
Bajolle, F.; Rose, J.P.; Leroux, B.; Teyssier, J.R.; Ferrand, J.; Fandre, M. 1980: Chromosome 18 partial duplication-deficiency by recombination aneusomia in familial pericentric inversion. Annales de Pediatrie 27(4): 241-244
Badalian, L.O.; Zhurba, L.G.; Koroleva, I.A.; Aĭngorn, E.D.; Veshneva, I.V. 1972: Chromosome 18 trisomy syndrome. Pediatriia 51(3): 56-59
Berger, B. 1972: Chromosome 18. Structural abnormalities. Ii. La Nouvelle Presse Medicale 1(10): 663-664
Berger, R. 1972: Chromosome 18. Structure abnormalities. i. La Nouvelle Presse Medicale 1(9): 598-600
Knuutila, S.; Ruutu, T.; Partanen, S.; Vuopio, P. 1983: Chromosome 1q+ in erythroid and granulocyte-monocyte precursors in a patient with essential thrombocythemia. Cancer Genetics and Cytogenetics 9(3): 245-249
Babu, V.R.; Van Dyke, D.L.; Jackson, C.E. 1984: Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study. Proceedings of the National Academy of Sciences of the United States of America 81(8): 2525-2528
Bernstein, R.; Pinto, M.R.; Behr, A.; Mendelow, B. 1982: Chromosome 3 abnormalities in acute nonlymphocytic leukemia (ANLL) with abnormal thrombopoiesis: report of three patients with a "new" inversion anomaly and a further case of homologous translocation. Blood 60(3): 613-617
Miller, Y.E.; Jones, C.; Scoggin, C.; Morse, H.; Seligman, P. 1983: Chromosome 3q (22-ter) encodes the human transferrin receptor. American Journal of Human Genetics 35(4): 573-583
Berger, A.; Dar, H.; Reiter, A.; Tal, Y. 1983: Chromosome 4q deletion syndrome: a case report. Israel Journal of Medical Sciences 19(9): 850-852
Pasquali, F.; Maraschio, P.; Zara, C. 1973: Chromosome 6/17 translocation as a cause of repeated abortions. Annali di Ostetricia Ginecologia Medicina Perinatale 94(9-10): 553-559
Reichmann, A.; Martin, P.; Levin, B. 1984: Chromosome 6q- in metastatic melanoma involving the large bowel. Cancer Genetics and Cytogenetics 13(3): 275-277
Scheres, J.M.; Hustinx, T.W.; Weemaes, C.M. 1980: Chromosome 7 in ataxia-telangiectasia. Journal of Pediatrics 97(3): 440-441
Rogóyski, A.; Babel, M.; Tronowska, T.D. 1982: Chromosome 8 trisomy in an infant. Pediatria Polska 57(5-6): 425-427
Rogóyski, A.; Babel, M.; Jabłońska-Skwiecińska, E.; Tronowska, T.D.; Sienicka, M. 1984: Chromosome 8 trisomy in mosaicism (46,XX/47, + 8). Pediatria Polska 59(2): 135-138
Miyamoto, K.; Sato, J.; Kitajima, K.; Hiraki, S.; Mori, K.; Tanaka, T. 1982: Chromosome 8-14 translocation in a non-African Burkitt's lymphoma with leukemic conversion. Acta Medica Okayama 36(2): 157-160
Einhorn, S.; Heyman, M. 1993: Chromosome 9 short arm deletions in malignant diseases. Leukemia and Lymphoma 11(3-4): 191-196
Tiepolo, L.; Zara, C.; Fraccaro, M. 1967: Chromosome DNA replication in human tumour cells labelled in vivo and in vitro. European Journal of Cancer 3(4): 355-360
Cathelineau, L.; Saudubray, J.M.; Navarro, J.; Polonovski, C. 1973: Chromosome X transmission of the ornithine-carbamyl-transferase structural gene. a study of 3 families. Annales de Genetique 16(3): 173-182
Zara, C.; Tiepolo, L. 1970: Chromosome X triploidy detected by chance in pregnancy. Annali di Ostetricia Ginecologia Medicina Perinatale 92(6): 391-395
Krzyzowski, J.; Wasilewski, B. 1971: Chromosome y abnormalities and their psychopathological aequelae. Psychiatria Polska 5(4): 465-468
Parcheta, B.; Skawiński, W.; Wiśniewski, L. 1982: Chromosome y polymorphism in genital organ abnormalities. Polski Tygodnik Lekarski 37(21): 609-611
Wolff, S. 1972: Chromosome abberations induced by ultraviolet radiation. Photophysiology 7: 189-205
Berger, R. 1970: Chromosome aberations and ionizing radiations. Revue Europeenne d'Etudes Cliniques et Biologiques. European Journal of Clinical and Biological Research 15(4): 375-381
Pfeiffer, R.A.; Wilking, H.H.; Manz, F.; Krienitz, B. 1973: Chromosome aberration 48, XXXY. Munchener Medizinische Wochenschrift 115(14): 594-598
Asaka, A. 1972: Chromosome aberration and mental retardation. Shinkei Kenkyu no Shimpo. Advances in Neurological Sciences 16(2): 226-231
Novikov, I.I.; Slozina, N.M.; Borovitskaia, E.E.; Golovachev, G.D. 1981: Chromosome aberration and sister chromatid exchange study of female workers in the rubber industry. Akusherstvo i Ginekologiia 1981(1): 22-23
Grant, W.F. 1982: Chromosome aberration assays in Allium. A report of the U.S. Environmental Protection Agency Gene-Tox Program. Mutation Research 99(3): 273-291
Barnes, C.A.; Holmes, H.L.; Ilbery, P.L. 1969: Chromosome aberration following radiophosphorus treatment of polycythaemia. Australasian Radiology 13(4): 396-417
Sasaki, M.S. 1980: Chromosome aberration formation and sister chromatid exchange in relation to DNA repair in human cells. Basic Life Sciences 15: 285-313
Piatkin, E.K.; Pokrovskaia, V.N.; Triska, V.V. 1980: Chromosome aberration frequency in human bone marrow and peripheral blood lymphocyte cultures after in vitro gamma irradiation. Meditsinskaia Radiologiia 25(2): 44-49
Aleksandrov, S.E. 1982: Chromosome aberration frequency in workers in tire and industrial ruber manufacture. Genetika 18(1): 161-163
Bauchinger, M.; Schmid, E. 1973: Chromosome aberration in human lymphocytes after X-irradiation in vitro. II. Analysis of primary processes in the formation of dicentric chromosomes. Mutation Research 20(1): 107-113
Gorbumova, L.V.; Varshaver, N.B.; Lelikova, G.P.; Shapiro, N.I. 1981: Chromosome aberration induction by a temperature-sensitive SV40 mutant in mammalian cells. Nauchnye Doklady Vysshei Shkoly. Biologicheskie Nauki 1981(10): 75-78
Volnianskaia, A.V.; Vasilos, A.F. 1981: Chromosome aberration level in agricultural workers. Gigiena Truda i Professional'nye Zabolevaniya (12): 47-48
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Ishidate, M.; Yoshikawa, K. 1980: Chromosome aberration tests with Chinese hamster cells in vitro with and without metabolic activation--a comparative study on mutagens and carcinogens. Archives of Toxicology. Supplement. 4: 41-44
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Nielsén, K.; Granzow, C. 1983: Chromosome band patterns of near tetraploid Ehrlich-Lettré mouse ascites cells (ELT Bonn) in vivo and in vitro. Hereditas 98(1): 95-103
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Hori, T.; Ayusawa, D.; Shimizu, K.; Koyama, H.; Seno, T. 1984: Chromosome breakage induced by thymidylate stress in thymidylate synthase-negative mutants of mouse FM3A cells. Cancer Research 44(2): 703-709
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Chen, T.R. 1983: Chromosome changes in 6-TG-resistant mutant strains derived from a karyotypically stable human line, C32. Cytogenetics and Cell Genetics 35(3): 181-189
Buckton, K.E.; Whalley, L.J.; Lee, M.; Christie, J.E. 1983: Chromosome changes in Alzheimer's presenile dementia. Journal of Medical Genetics 20(1): 46-51
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Frolov, A.K. 1983: Chromosome changes in the blood lymphocytes compared to the strength of the immunity in parotitis virus infection and vaccination. Tsitologiia i Genetika 17(6): 27-32
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