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Journal of the American Dental Association (1939)|November 1, 1983
Epidermolysis bullosa--review and report of caseD L Carroll, M J Stephan, G L HaysGenomics|August 11, 1992
Deletion mapping of H-Y antigen to the long arm of the human Y chromosomeM A Cantrell, J S Bogan, E Simpson, et al.Pediatric Research|September 1, 1990
Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathyI Tein, D C De Vivo, F Bierman, et al.Annales De Genetique|January 1, 1987
Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotypeC N Onufer, M J Stephan, H C Thuline, et al.Journal of Pediatric Ophthalmology and Strabismus|March 1, 1988
Enlarged pupillary membranesT H Mader, F L Wergeland, K J Chismire, et al.American Journal of Medical Genetics|August 26, 1998
Variant RSH/Smith-Lemli-Opitz syndrome with atypical sterol metabolismA J Anderson, M J Stephan, W O Walker, et al.The Journal of Pediatrics|June 1, 1980
Limb reduction anomalies and early in utero limb compressionJ M Graham, M E Miller, M J Stephan, et al.The Journal of Pediatrics|September 1, 1975
Macrocephaly in association with unusual cutaneous angiomatosisM J Stephan, B D Hall, D W Smith, et al.American Journal of Medical Genetics|June 1, 1994
Hypothalamic hamartoma in oral-facial-digital syndrome type VI (Váradi syndrome)M J Stephan, K L Brooks, D C Moore, et al.American Journal of Medical Genetics|December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated familiesR M Hughes-Benzie, G Pilia, J Y Xuan, et al.Pageof 9