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Human Molecular Genetics|July 21, 1998
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defectsK Sossey-Alaoui, A J Hartung, R Guerrini, 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|July 31, 1995
Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individualsM C Phelan, R C Rogers, K B Clarkson, 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.American Journal of Medical Genetics|December 1, 1985
An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcaneiW R Osebold, D J Remondini, E L Lester, et al.International Journal of Cardiology|January 1, 1989
Coexistent cardiac tumours and malformations of the heartG A Russell, J P Dhasmana, P J Berry, et al.Pediatric Pathology|January 1, 1985
Angiosarcoma of the liver and spleen in an infantB Alt, G R Hafez, M Trigg, et al.Archives of Pathology & Laboratory Medicine|September 1, 1983
Hunter' syndrome. Ultrastructural features in young childrenJ V Murphy, A E Hodach, E F Gilbert, et al.Pageof 40