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Human Genetics|May 1, 2012
Epidemiology of substance use disordersKathleen R Merikangas, Vetisha L McClairHuman Genetics|December 1, 1990
Assignment of human tracheobronchial mucin gene(s) to 11p15 and a tracheobronchial mucin-related sequence to chromosome 13V C Nguyen, J P Aubert, M S Gross, et al.Human Genetics|December 1, 1990
Assignment of the gene for central core disease to chromosome 19E A Haan, C J Freemantle, J A McCure, et al.Human Genetics|December 1, 1990
The major cystic fibrosis mutation in a British populationC J McMahon, S A Genet, H R Middleton-Price, et al.Human Genetics|December 4, 2013
Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variantsCan Yang, Cong Li, Henry R Kranzler, et al.Human Genetics|November 1, 1986
Leftward deletion alpha-thalassaemia in the Saudi Arabian populationM A el-HazmiHuman Genetics|November 6, 2013
Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNAMadalene A Earp, Linda E Kelemen, Anthony M Magliocco, et al.Human Genetics|September 1, 1986
Hemoglobin abnormalities. An evaluation on new-born infants and their mothers in a maternity unit close to Brazzaville (P.R. Congo)M Lallemant, F Galacteros, S Lallemant-Lecoeur, et al.Human Genetics|November 28, 2013
COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal laminaJuan Arredondo, Marian Lara, Fiona Ng, et al.Pageof 957