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European Journal of Human Genetics : EJHG|August 22, 2000
Exclusion of the Ellis-van Creveld region on chromosome 4p16 in some families with asphyxiating thoracic dystrophy and short-rib polydactyly syndromesD Krakow, D Salazar, W R Wilcox, et al.American Journal of Medical Genetics|April 29, 1998
Lethal syndrome of skeletal dysplasia and progressive central nervous system degenerationM Khosravi, D D Weaver, M J Bull, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1996
Short-term recombinant human growth hormone treatment increases growth rate in achondroplasiaM Shohat, D Tick, S Barakat, et al.Plastic and Reconstructive Surgery|March 1, 1981
Familial lymphedema praecox: Meige's diseaseE S Wheeler, V Chan, R Wassman, et al.The American Journal of Pathology|July 1, 1985
Pathologic findings in adenosine deaminase-deficient severe combined immunodeficiency. I. Kidney, adrenal, and chondro-osseous tissue alterationsH Ratech, M A Greco, G Gallo, et al.American Journal of Human Genetics|November 1, 1983
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneityS E Hodge, C E Anderson, K Neiswanger, et al.American Journal of Medical Genetics|August 1, 1985
The role of mesenchyme-like tissue in the pathogenesis of thanatophoric dysplasiaA Ornoy, G E Adomian, D J Eteson, et al.Genetic Epidemiology|January 1, 1984
No evidence for linkage between an insulin-dependent diabetes mellitus-susceptibility locus and immunoglobulin loci KM or GML L Field, A Goldstein, M A Spence, et al.American Journal of Medical Genetics|September 1, 1982
Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasiaD O Sillence, R S Lachman, T Jenkins, et al.American Journal of Medical Genetics|September 1, 1986
A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasiaZ Borochowitz, K L Jones, R Silbey, et al.Pageof 42