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American Journal of Medical Genetics|September 1, 1990
Rokitansky sequence in association with the facio-auriculo-vertebral sequence: part of a mesodermal malformation spectrum?E A Wulfsberg, T M GrigbsyAmerican Journal of Medical Genetics|September 1, 1993
"Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrumI W Lurie, E A WulfsbergGenetic Counseling (Geneva, Switzerland)|January 1, 1994
The McKusick-Kaufman syndrome: phenotypic variation observed in familial cases as a clue for the evaluation of sporadic casesI W Lurie, E A WulfsbergClinical Pediatrics|May 1, 1986
Duchenne muscular dystrophy in a 46 XY femaleE A Wulfsberg, R R SkoglundJournal of Developmental and Behavioral Pediatrics : JDBP|August 1, 1992
A complex chromosome rearrangement in a boy with autismJ O Lopreiato, E A WulfsbergAmerican Journal of Medical Genetics|July 15, 1992
Chondrodysplasia punctata: a boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disordersE A Wulfsberg, J Curtis, C H JayneClinical Genetics|July 1, 1991
The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot with pulmonary atresiaE A Wulfsberg, E J Zintz, J W MooreClinical Dysmorphology|January 1, 1994
The acrocallosal syndrome: expansion of the phenotypic spectrumI W Lurie, I V Naumchik, E A WulfsbergAmerican Journal of Medical Genetics|June 15, 1993
Autosomal dominant tetramelic postaxial oligodactylyE A Wulfsberg, L J Mirkinson, S J MeisterClinical Genetics|May 1, 1991
Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasiaE A Wulfsberg, W C Wassel, C A PoloPageof 3