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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.
American Journal of Medical Genetics|August 22, 2000
Genetic epidemiological study of keratoconus: evidence for major gene determinationY Wang, Y S Rabinowitz, J I Rotter, et al.
Genetic Epidemiology|January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disordersX Bu, H Y Yang, M Shohat, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 1, 1993
Helicobacter pylori, pepsinogen, and risk for gastric adenocarcinomaJ Parsonnet, I M Samloff, L M Nelson, 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.
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