X linked dominant chondrodysplasia punctata happle syndrome in a boy
Tronnier, M.; Froster Iskenius, U.G.; Schmeller, W.; Happle, R.; Wolff, H.H.
Hautarzt 43(4): 221-225
1992
ISSN/ISBN: 0017-8470
Accession: 034253010
PDF emailed within 1 workday: $29.90
Related References
Jacyk, W.K. 2001: What syndrome is this? X-linked dominant chondrodysplasia punctata (Happle) Pediatric Dermatology 18(5): 442-444Sutphen, R.; Amar, M.J.; Kousseff, B.G.; Toomey, K.E. 1995: XXY male with X-linked dominant chondrodysplasia punctata (Happle syndrome) American Journal of Medical Genetics 57(3): 489-492
Froster Iskenius, U.G.; Tronnier, M.; Schmeller, W.; Happle, R.; Wolff, H. 1991: X linked dominant chondrodysplasia punctata happle syndrome in a male? Clinical Genetics 40(5): 381
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Yanagihara, M.; Ueda, K.; Asano, N.; Ozawa, T.; Nakatani, A.; Hirose, M. 1996: Usefulness of histopathologic examination of thick scales in the diagnosis of X-linked dominant chondrodysplasia punctata (Happle) Pediatric Dermatology 13(1): 1-4
Schutgens, R.B.H.; Heymans, H.S.A.; Wanders, R.J.A.; Oorthuys, J.W.E.; Tager, J.M.; Schrakamp, G.; Van Den Bosch, H.; Beemer, F.A. 1988: Multiple peroxisomal enzyme deficiencies in rhizomelic chondrodysplasia punctata comparison with zellweger syndrome conradi huenermann syndrome and the x linked dominant type of chondrodysplasia punctata Goldberg, D M , Et Al (Ed ) Advances in Clinical Enzymology, Vol 6 Enzymes: Tools And Targets; 6th International Congress, Hannover, West Germany, September 16-19, 1987 Viii+272p S Karger Ag: Basel, Switzerland; New York, New York, Usa Illus 57-65
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Tronnier, M.; Froster-Iskenius, U.G.; Schmeller, W.; Happle, R.; Wolff, H.H. 1992: X-chromosome dominant chondrodysplasia punctata (Happle) in a boy Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 43(4): 221-225