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The Journal of Pediatrics|August 1, 1977
Dominant inheritance of cerebral gigantismJ Zonana, J F Sotos, C A Romshe, et al.American Journal of Human Genetics|February 1, 1996
Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasiasJ Hästbacka, A Superti-Furga, W R Wilcox, et al.American Journal of Medical Genetics|March 1, 1986
Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneityD O Sillence, K K Barlow, W G Cole, et al.American Journal of Medical Genetics|March 1, 1988
A new autosomal recessive lethal chondrodystrophy with congenital hydropsC R Greenberg, D L Rimoin, H E Gruber, et al.American Journal of Medical Genetics|May 26, 1998
Pacman dysplasia: report of two affected sibsW R Wilcox, B C Lucas, B Loebel, et al.Matrix Biology : Journal of the International Society for Matrix Biology|November 20, 1998
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate productionA Rossi, I Kaitila, W R Wilcox, et al.American Journal of Medical Genetics|July 1, 1994
Increased risk for type I (insulin-dependent) diabetes in relatives of patients with alopecia areata (AA)S J Wang, T Shohat, C Vadheim, et al.American Journal of Human Genetics|November 1, 1982
Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortionB D Blumberg, J D Shulkin, J I Rotter, et al.American Journal of Human Genetics|January 1, 1995
Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locusC A DeMeester, X Bu, R J Gray, et al.American Journal of Medical Genetics|January 30, 1995
Arthrogryposis multiplex congenita in an Arab kindred: updateL Jaber, R Weitz, X Bu, et al.Pageof 42