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Journal of Human Genetics|January 19, 2006
De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathologySergey I Zhadanov, Vasiliy V Atamanov, Nikolay I Zhadanov, et al.
Journal of Human Genetics|January 24, 2006
Association of IL8, CXCR2 and TNF-alpha polymorphisms and airway diseaseMelanie C Matheson, Justine A Ellis, Joan Raven, et al.
Journal of Human Genetics|April 2, 2008
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth diseasePaola Mandich, Marina Grandis, Alessandro Geroldi, et al.
Journal of Human Genetics|April 17, 2008
Genome-wide linkage analysis for circulating levels of adipokines and C-reactive protein in the Quebec family study (QFS)Stephanie-May Ruchat, Jean-Pierre Després, S John Weisnagel, et al.
Journal of Human Genetics|April 17, 2008
Subsequent pregnancy outcomes in recurrent miscarriage patients with a paternal or maternal carrier of a structural chromosome rearrangementMayumi Sugiura-Ogasawara, Koji Aoki, Tomoyuki Fujii, et al.
Journal of Human Genetics|April 17, 2008
Analysis of regulatory polymorphisms in organic ion transporter genes (SLC22A) in the kidneyKen Ogasawara, Tomohiro Terada, Hideyuki Motohashi, et al.
Journal of Human Genetics|March 20, 2008
The role of MTHFR gene in multiple myelomaElias Zintzaras, Stavroula Giannouli, Paraskevi Rodopoulou, et al.
Journal of Human Genetics|March 20, 2008
Analysis of GADD45A sequence variations in French Canadian families with high risk of breast cancerSylvie Desjardins, Geneviève Ouellette, Yvan Labrie, et al.
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