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Annual Review of Genomics and Human Genetics|June 12, 2008
From linkage maps to quantitative trait loci: the history and science of the Utah genetic reference projectStephen M Prescott, Jean Marc Lalouel, Mark Leppert
Human Genetics|September 1, 2004
A longitudinal study of X-inactivation ratio in human femalesIonel Sandovici, Anna K Naumova, Mark Leppert, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2006
Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutationAmy F Hubbard, E Wayne Askew, Nanda Singh, et al.
Science (New York, N.Y.)|February 22, 2003
Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamideUn-kyung Kim, Eric Jorgenson, Hilary Coon, et al.
Human Molecular Genetics|June 19, 2003
Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regionsIonel Sandovici, Mark Leppert, Patricia Red Hawk, et al.
The Journal of Infectious Diseases|January 18, 2008
Identification of a herpes simplex labialis susceptibility region on human chromosome 21Maurine R Hobbs, Brandt B Jones, Brith E Otterud, et al.
Plos Genetics|July 15, 2006
Human imprinted chromosomal regions are historical hot-spots of recombinationIonel Sandovici, Sacha Kassovska-Bratinova, Joe E Vaughan, et al.
Molecular Neuropsychiatry|November 22, 2016
A Rare Variant in <i>CACNA1D</i> Segregates with 7 Bipolar I Disorder Cases in a Large PedigreeJessica Ross, Erika Gedvilaite, Judith A Badner, et al.
Investigative Ophthalmology & Visual Science|January 31, 2002
Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblingsPaul S Bernstein, Mark Leppert, Nanda Singh, et al.
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