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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.Diabetes|February 1, 1983
HLA genotypic study of insulin-dependent diabetes the excess of DR3/DR4 heterozygotes allows rejection of the recessive hypothesisJ I Rotter, C E Anderson, R Rubin, et al.American Journal of Medical Genetics|November 1, 1982
Spondylometepiphyseal dysplasia, Strudwick typeC E Anderson, D O Sillence, R S Lachman, et al.American Journal of Medical Genetics|March 27, 1995
Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndromeG Kohn, G Malinger, R el Shawwa, et al.American Journal of Medical Genetics|February 1, 1985
Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasiaT G Brewster, R S Lachman, D C Kushner, et al.Pageof 42