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Blood Cells, Molecules & Diseases|January 1, 1996
Localization of the hemochromatosis disease gene: linkage disequilibrium analysis using an American patient collectionN K Seese, C P Venditti, K A Chorney, et al.
Hepatology (Baltimore, Md.)|February 15, 2001
Uroporphyria in Hfe mutant mice given 5-aminolevulinate: a new model of Fe-mediated porphyria cutanea tardaP R Sinclair, N Gorman, H S Walton, et al.
Journal of Medical Genetics|January 1, 1997
46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosisC P Venditti, N K Seese, G S Gerhard, et al.
International Journal of Obesity (2005)|August 17, 2013
Gene expression profiling in subcutaneous, visceral and epigastric adipose tissues of patients with extreme obesityG S Gerhard, A M Styer, W E Strodel, et al.
Blood Cells, Molecules & Diseases|January 1, 1996
Mutation analysis in hereditary hemochromatosisE Beutler, T Gelbart, C West, et al.
Genes, Brain, and Behavior|August 13, 2009
Genetic architecture for hole-board behaviors across substantial time intervals in young, middle-aged and old miceJ E Foreman, A Lionikas, D H Lang, et al.
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