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American Journal of Human Genetics|May 13, 2003
A neutral explanation for the correlation of diversity with recombination rates in humansInes Hellmann, Ingo Ebersberger, Susan E Ptak, et al.American Journal of Human Genetics|July 5, 2003
Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genomeAndrew G Clark, Rasmus Nielsen, James Signorovitch, et al.American Journal of Human Genetics|July 10, 2003
The International Psoriasis Genetics Study: assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairsAmerican Journal of Human Genetics|October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasiaW A Sweetman, B Rash, B Sykes, et al.American Journal of Human Genetics|August 16, 2003
An integrated haplotype map of the human major histocompatibility complexEmily C Walsh, Kristie A Mather, Stephen F Schaffner, et al.American Journal of Human Genetics|September 16, 2003
Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosisOonagh Dowling, Analisa Difeo, Maria C Ramirez, et al.American Journal of Human Genetics|July 1, 1976
Cytogenetic darkroom magic: now you see them, now you don'tK M Overton, R E Magenis, T Brady, et al.American Journal of Human Genetics|December 1, 1992
Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5qS G Ryan, M J Dixon, M A Nigro, et al.American Journal of Human Genetics|August 6, 2003
The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in spermRivka L Glaser, Karl W Broman, Rebecca L Schulman, et al.American Journal of Human Genetics|December 1, 1992
Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)L Boulet, G Karpati, E A ShoubridgePageof 979