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Pediatrics|July 1, 1987
Williams syndrome: features in late childhood and adolescenceR A Pagon, F C Bennett, B LaVeck, et al.
Clinical Dysmorphology|April 18, 1998
Brachydactyly type A1 with abnormal menisci and scoliosis in three generationsM L Raff, K A Leppig, J C Rutledge, et al.
American Journal of Medical Genetics|June 15, 1993
Mosaic isochromosome 8pD J Tilstra, M Grove, A C Spencer, et al.
American Journal of Medical Genetics|January 1, 1990
Partial deletion of the long arm of chromosome 11 [del(11)(q23.3----qter)] with abnormal white matterT D Wardinsky, E Weinberger, R A Pagon, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three familiesY Tatuch, R A Pagon, B Vlcek, et al.
The Journal of Pediatrics|September 1, 1996
Prevalence of hypopigmented macules in a healthy populationS L Vanderhooft, J S Francis, R A Pagon, et al.
Proceedings. AMIA Symposium|February 3, 1999
Creation and maintenance of Helix, a Web based database of medical genetics laboratories, to serve the needs of the genetics communityP Tarczy-Hornoch, M L Covington, J Edwards, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 1, 1991
Nasal dermoid sinus cysts: association with intracranial extension and multiple malformationsT D Wardinsky, R A Pagon, R J Kropp, et al.
American Journal of Medical Genetics|May 8, 2000
Two novel fibrillin-2 mutations in congenital contractural arachnodactylyS Belleh, G Zhou, M Wang, et al.
Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.
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