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Browse Human genetics topic

Genetic aspects subtopic


1-9 out of 9 article(s)
Title Author Type Date Words
An unusual case of severe hypertriglyceridemia and splenomegaly. Rahalkar, Amit R.; Wang, Jian; Sirrs, Sandra; Dimmick, James; Holmes, Daniel; Urquhart, Nadine; Hege Mar 1, 2008 3263
Validation of a CYP2D6 genotyping panel on the NanoChip molecular biology workstation. Lee, Hong-Kee; Lewis, Lionel D.; Tsongalis, Gregory J.; Schur, Bernard C.; Jannetto, Paul J.; Wong, May 1, 2007 4094
Homocysteine, 5, 10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24 968 initially healthy women. Zee, Robert Y.L.; Mora, Samia; Cheng, Suzanne; Erlich, Henry A.; Lindpaintner, Klaus; Rifai, Nader; Clinical report May 1, 2007 5941
Multiplex assays with fluorescent microbead readout: a powerful tool, for mutation detection. Ugozzoli, Luis A. Nov 1, 2004 3077
Detection of prevalent genetic alterations predisposing to hemochromatosis and other common human diseases. Press, Richard D. Oct 1, 2000 2193
Single-nucleotide polymorphisms in intron 2 of CYP21P: evidence for a higher rate of mutation at CpG dinucleotides in the functional steroid 21-hydroxylase gene and application to segregation analysis in congenital adrenal hyperplasia. Jiddou, Renee R.; Wei, Wan-li; Sane, Kumud S.; Killeen, Anthony A. May 1, 1999 3359
CYPs, SNPs, and molecular diagnosis in the postgenomic era. Vilain, Eric Dec 1, 1998 1402
Automated fluorescent analysis procedure for enzymatic mutation detection. Del Tito, Benjamin J., Jr.; Poff, Herbert E., III; Novotny, Mark A.; Cartledge, Donna M.; Walker, Ra Clinical report Apr 1, 1998 4196
Pharmacogenetics: a laboratory tool for optimizing therapeutic efficiency. Linder, Mark W.; Prough, Russell A.; Valdes, Roland Jr. Feb 1, 1997 10304

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