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American Journal of Medical Genetics|January 1, 1987
Progressive form of multiple pterygium syndrome in association with nemalin-myopathy: report of a female followed for twelve yearsF Papadia, N Longo, L Serlenga, et al.American Journal of Medical Genetics|January 1, 1987
Dominant inheritance of a syndrome similar to Rubinstein-TaybiP Cotsirilos, J C Taylor, R MatalonAmerican Journal of Medical Genetics|February 1, 1987
Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patientsB R Rollnick, C I Kaye, K Nagatoshi, et al.American Journal of Medical Genetics|February 1, 1987
Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiencyD S Rosenblatt, I T Thomas, D Watkins, et al.American Journal of Medical Genetics|February 25, 1998
Omphalocele with absent radial ray (ORR): a case with diploid-triploid mixoploidyH J Lin, B Schaber, C H Hashimoto, et al.American Journal of Medical Genetics|February 25, 1998
Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classificationN H Robin, J A Scott, J E Arnold, et al.American Journal of Medical Genetics|February 25, 1998
Novel mutation in the FGFR2 gene at the same codon as the Crouzon syndrome mutations in a severe Pfeiffer syndrome type 2 caseF Schaefer, C Anderson, B Can, et al.American Journal of Medical Genetics|February 25, 1998
SAMS: provisionally unique multiple congenital anomalies syndrome consisting of short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalitiesE G Lemire, G E Hildes-Ripstein, M H Reed, et al.American Journal of Medical Genetics|February 25, 1998
Tall stature, microcephaly, hypotonia, advanced bone age, and unusual infra-auricular creasesR F StrattonAmerican Journal of Medical Genetics|February 25, 1998
Central nervous system malformations in ethylmalonic encephalopathyM J Nowaczyk, S I Blaser, J T ClarkePageof 854