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American Journal of Medical Genetics|March 15, 1996
Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toesN H Robin, B Segel, G Carpenter, et al.American Journal of Medical Genetics|March 29, 1996
Thomas syndrome: potter sequence with cleft lip/palate and cardiac anomaliesJ Zlotogora, I Ariel, A Ornoy, et al.American Journal of Medical Genetics|March 29, 1996
Two sibs with anophthalmia and pulmonary hypoplasia (the Matthew-Wood syndrome)M J Seller, T B Davis, C N Fear, et al.American Journal of Medical Genetics|March 29, 1996
Mental retardation, epilepsy, short stature, and skeletal dysplasia: confirmation of the Gurrieri syndromeA Battaglia, E Orsitto, G GibiliscoAmerican Journal of Medical Genetics|March 29, 1996
Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndromeJ S Fryburg, K Y Lin, W L GoldenAmerican Journal of Medical Genetics|March 29, 1996
Genetic study of scaphocephalyE Lajeunie, M Le Merrer, C Bonaïti-Pellie, et al.American Journal of Medical Genetics|March 29, 1996
Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2)L Potocki, L G ShafferAmerican Journal of Medical Genetics|February 2, 1996
Autosomal dominant transmission of familial laterality defectsB Casey, B F Cuneo, C Vitali, et al.American Journal of Medical Genetics|February 2, 1996
Pedigree analysis in families with febrile seizuresW G Johnson, S L Kugler, E S Stenroos, et al.American Journal of Medical Genetics|February 2, 1996
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.Pageof 854