Showing results (791-800 of 9,786) with videos related to
Sort By:
Pageof 979
American Journal of Human Genetics|October 1, 1996
Origin and evolution of Native American mtDNA variation: a reappraisalP Forster, R Harding, A Torroni, et al.American Journal of Human Genetics|October 1, 1996
Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypesH Zhang, N RischAmerican Journal of Human Genetics|October 3, 1998
Multiple phenotype modeling in gene-mapping studies of quantitative traits: power advantagesD B Allison, B Thiel, P St Jean, et al.American Journal of Human Genetics|October 3, 1998
Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysisS G Schwab, J Hallmayer, B Lerer, et al.American Journal of Human Genetics|October 3, 1998
Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33J D Rioux, V A Stone, M J Daly, et al.American Journal of Human Genetics|October 3, 1998
A gene for Meckel syndrome maps to chromosome 11q13J Roume, E Genin, V Cormier-Daire, et al.American Journal of Human Genetics|October 3, 1998
Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolutionO El-Maarri, A Olek, B Balaban, et al.American Journal of Human Genetics|October 3, 1998
Linkage disequilibrium mapping of the gene for Margarita Island ectodermal dysplasia (ED4) to 11q23K Suzuki, T Bustos, R A SpritzAmerican Journal of Human Genetics|December 5, 1998
The first nuclear-encoded complex I mutation in a patient with Leigh syndromeJ Loeffen, J Smeitink, R Triepels, et al.American Journal of Human Genetics|December 5, 1998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiencyV Tiranti, K Hoertnagel, R Carrozzo, et al.Pageof 979