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American Journal of Human Genetics|August 11, 2004
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility regionP Paschou, Y Feng, A J Pakstis, et al.American Journal of Human Genetics|September 14, 2000
Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human originsS A Tishkoff, A J Pakstis, M Stoneking, et al.Nucleic Acids Research|January 10, 2003
ALFRED: the ALelle FREquency Database. UpdateH Rajeevan, M V Osier, K-H Cheung, et al.Human Genetics|October 6, 1998
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locusK K Kidd, B Morar, C M Castiglione, et al.Journal of the American Medical Informatics Association : JAMIA|November 1, 1995
Internet-based support for bioscience research: a collaborative genome center for human chromosome 12P L Miller, P M Nadkarni, K K Kidd, et al.Annals of Human Genetics|March 30, 2000
Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative studyL Quintana-Murci, O Semino, E S Poloni, et al.Oncogene|December 2, 2010
A Variant in a MicroRNA complementary site in the 3' UTR of the KIT oncogene increases risk of acral melanomaS E Godshalk, T Paranjape, S Nallur, et al.Human Molecular Genetics|September 25, 1997
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1T S Breschel, M G McInnis, R L Margolis, et al.Forensic Science International. Genetics|August 5, 2019
MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populationsC Phillips, D McNevin, K K Kidd, et al.Molecular Psychiatry|April 21, 2004
COMT haplotypes suggest P2 promoter region relevance for schizophreniaM A Palmatier, A J Pakstis, W Speed, et al.Pageof 22