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Human Genetics|July 19, 2005
CTLA4 is differentially associated with autoimmune diseases in the Dutch populationAlexandra Zhernakova, Peter Eerligh, Pilar Barrera, et al.Human Genetics|July 20, 2005
Use of autosomal loci for clustering individuals and populations of East Asian originJong-Jin Kim, Paul Verdu, Andrew J Pakstis, et al.Human Genetics|July 16, 2005
Complex HTR2C linkage disequilibrium and promoter associations with body mass index and serum leptinShane McCarthy, Salim Mottagui-Tabar, Yumi Mizuno, et al.Human Genetics|August 4, 2005
Maternal lineages and Alzheimer disease risk in the Old Order AmishJoelle M van der Walt, William K Scott, Susan Slifer, et al.Human Genetics|January 12, 2007
Genetic variation in tumor necrosis factor and lymphotoxin-alpha (TNF-LTA) and breast cancer riskMia M Gaudet, Kathleen M Egan, Jolanta Lissowska, et al.Human Genetics|April 17, 2007
Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generationBernie Devlin, Lambertus Klei, Marina Myles-Worsley, et al.Human Genetics|March 31, 2007
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese familyYoshinari Miyamoto, Tatsuo Matsuda, Hiroshi Kitoh, et al.Human Genetics|May 3, 2007
Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA familiesEmmanuelle Bouzigon, Ayse Ulgen, Marie-Hélène Dizier, et al.Human Genetics|May 4, 2007
Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than EuropeansM V Prasad Linga Reddy, Rafael Velázquez-Cruz, Vicente Baca, et al.Human Genetics|June 2, 2007
High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumorEric M Jackson, Tamim H Shaikh, Sridharan Gururangan, et al.Pageof 957