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American Journal of Human Genetics|July 15, 2003
Nuclear and mitochondrial DNA analysis of a 2,000-year-old necropolis in the Egyin Gol Valley of MongoliaChristine Keyser-Tracqui, Eric Crubézy, Bertrand LudesAmerican Journal of Human Genetics|January 1, 1976
The Diego blood groups: a genetic linkage analysisM Lewis, H Kaita, B Chown, et al.American Journal of Human Genetics|January 1, 1976
Evidence for "deleted" or "silent" genes homozygous at the locus coding for the constant region of the gamma3 chainG Lefranc, L Rivat, C Rivat, et al.American Journal of Human Genetics|December 13, 2002
The genetic origins of the Andaman IslandersPhillip Endicott, M Thomas P Gilbert, Chris Stringer, et al.American Journal of Human Genetics|May 23, 2003
Minimum description length block finder, a method to identify haplotype blocks and to compare the strength of block boundariesH Mannila, M Koivisto, M Perola, et al.American Journal of Human Genetics|May 15, 2012
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasetsIuliana Ionita-Laza, Vlad Makarov, , et al.American Journal of Human Genetics|April 3, 2012
On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacyHae Kyung Im, Eric R Gamazon, Dan L Nicolae, et al.American Journal of Human Genetics|April 3, 2012
Rare mutations in XRCC2 increase the risk of breast cancerD J Park, F Lesueur, T Nguyen-Dumont, et al.American Journal of Human Genetics|April 3, 2012
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication studyChristopher J Lessard, Indra Adrianto, John A Ice, et al.American Journal of Human Genetics|September 3, 2011
A general framework for detecting disease associations with rare variants in sequencing studiesDan-Yu Lin, Zheng-Zheng TangPageof 979