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Human Molecular Genetics|June 1, 1997
Molecular mechanisms in mitochondrial DNA depletion syndromeJ W Taanman, A G Bodnar, J M Cooper, et al.Human Molecular Genetics|June 1, 1997
A genome wide search for susceptibility loci in three European malignant hyperthermia pedigreesR L Robinson, N Monnier, W Wolz, et al.Human Molecular Genetics|March 26, 2002
STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair studyGabriele Duetsch, Thomas Illig, Sabine Loesgen, et al.Human Molecular Genetics|March 26, 2002
Linkage analysis of anorexia nervosa incorporating behavioral covariatesBernie Devlin, Silviu-Alin Bacanu, Kelly L Klump, et al.Human Molecular Genetics|March 26, 2002
The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle traffickingQing Zhang, Wei Li, Edward K Novak, et al.Human Molecular Genetics|April 25, 2002
Gene expression profiles of poor-prognosis primary breast cancer correlate with survivalFrançois Bertucci, Valéry Nasser, Samuel Granjeaud, et al.Human Molecular Genetics|April 25, 2002
Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 proteinJuha Isosomppi, Jouni Vesa, Anu Jalanko, et al.Human Molecular Genetics|April 25, 2002
Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorderCarol A Wise, Joseph D Gillum, Christine E Seidman, et al.Human Molecular Genetics|April 30, 2002
VSX1: a gene for posterior polymorphous dystrophy and keratoconusElise Héon, Alex Greenberg, Kelly K Kopp, et al.Human Molecular Genetics|April 30, 2002
Identification of transcriptional targets for Six5: implication for the pathogenesis of myotonic dystrophy type 1Shigeru Sato, Miwa Nakamura, Diane H Cho, et al.Pageof 1,196