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Human Genetics|April 2, 2023
Transcriptomic reprogramming for neuronal age reversalAlexandru M Plesa, Michael Shadpour, Ed Boyden, et al.Human Genetics|July 17, 2008
Reduced folate carrier 80A-->G polymorphism, plasma folate, and risk of placental abruptionCande V Ananth, Morgan R Peltier, Dirk F Moore, et al.Human Genetics|September 14, 2007
Methods to impute missing genotypes for population dataZhaoxia Yu, Daniel J SchaidHuman Genetics|July 1, 1991
Dominant mutations in familial lethal and severe osteogenesis imperfectaL Cohen-Solal, J Bonaventure, P MaroteauxHuman Genetics|July 1, 1991
T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detectionR P Ketterling, C D Bottema, D D Koeberl, et al.Human Genetics|June 26, 2008
Hereditary breast cancer: new genetic developments, new therapeutic avenuesPhilippe M Campeau, William D Foulkes, Marc D TischkowitzHuman Genetics|June 1, 1991
Exclusion of linkage to the pericentromeric region of chromosome 21 in the Canadian pedigree with familial Alzheimer diseaseS M Pulst, P Fain, V Cohn, et al.Human Genetics|June 30, 2006
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variantsJian-Min Chen, Claude Férec, David N CooperHuman Genetics|September 1, 1991
Polymorphisms of the gene encoding cholesterol ester transfer protein and serum lipoprotein levels in subjects with and without coronary heart diseaseH Tenkanen, P Koshinen, K Kontula, et al.Pageof 958