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American Journal of Medical Genetics|January 1, 1980
Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasiaJ W Spranger, A Schinzel, T Myers, et al.American Journal of Medical Genetics|October 21, 1999
Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactylyG K Hahm, R F Barth, G M Schauer, et al.Archives of Pathology & Laboratory Medicine|April 1, 1977
Sudden infant death due to congenital adrenal hypoplasiaM A Russell, J M Opitz, C Viseskul, et al.American Journal of Medical Genetics|June 8, 2001
Human anotocephaly (aprosopus, acrania-synotia) in the Vilnius anatomical collectionA Utkus, R Kazakevicius, R Ptasekas, et al.American Journal of Medical Genetics|January 1, 1977
The trisomy 4p syndrome: case report and reviewC H Gonzalez, A Sommer, L F Meisner, et al.American Journal of Medical Genetics|May 1, 1985
Ectopia cordis and cleft sternum: evidence for mechanical teratogenesis following rupture of the chorion or yolk sacL C Kaplan, R Matsuoka, E F Gilbert, et al.American Journal of Medical Genetics|June 8, 2001
Klippel-Feil anomaly with Sprengel anomaly, omovertebral bone, thumb abnormalities, and flexion-crease changes: novel association or syndrome?A R Larson, K D Josephson, R M Pauli, et al.American Journal of Medical Genetics|August 22, 1997
Familial broad terminal phalanges with one individual showing additional anomaliesL Pavone, G Sorge, V Pavone, et al.American Journal of Medical Genetics|March 13, 1995
Asplenia in two father-son pairsN M Lindor, W A Smithson, C A Ahumada, et al.Fetal and Pediatric Pathology|June 7, 2006
"Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndromeL G Best, E Gilbert-Barness, D E Gerrard, et al.Pageof 17