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Disease Markers|October 1, 1989
Application of synthetic oligonucleotides to detect DQ beta genes transmission within insulin-dependent diabetes familiesH Toyoda, M Onohara-Toyoda, J Krull, et al.The Journal of Clinical Investigation|March 1, 1997
Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypesG M Dallinga-Thie, M van Linde-Sibenius Trip, J I Rotter, et al.Nature Genetics|March 1, 1995
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3P L Tavormina, R Shiang, L M Thompson, et al.Diabetes Care|July 1, 1989
Different HLA haplotypes in Mexican Americans with IDDMC M Vadheim, A Zeidler, J I Rotter, et al.American Journal of Medical Genetics|July 16, 1999
Small deletions in the type II collagen triple helix produce kniest dysplasiaD J Wilkin, A S Artz, S South, et al.Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.Inflammatory Bowel Diseases|December 1, 1999
A genome-wide search identifies potential new susceptibility loci for Crohn's diseaseY Ma, J D Ohmen, Z Li, et al.Gastroenterology|June 1, 1996
Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroupE A Vasiliauskas, S E Plevy, C J Landers, et al.American Journal of Medical Genetics|June 19, 1998
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutationY Bykhovskaya, M Shohat, K Ehrenman, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|November 13, 1999
Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16qB E Aouizerat, H Allayee, R M Cantor, et al.Pageof 42