Showing results (1341-1350 of 9,569) with videos related to
Sort By:
Pageof 957
Human Genetics|June 1, 2005
Fabry disease: correlation between structural changes in alpha-galactosidase, and clinical and biochemical phenotypesFumiko Matsuzawa, Sei-ichi Aikawa, Hirofumi Doi, et al.Human Genetics|May 11, 2005
Molecular characterisation of the pericentric inversion that distinguishes human chromosome 5 from the homologous chimpanzee chromosomeJustyna M Szamalek, Violaine Goidts, Nadia Chuzhanova, et al.Human Genetics|July 28, 2004
Association between evolutionary history of angiotensinogen haplotypes and plasma levelsLaura Fejerman, Nourdine Bouzekri, Xiaodong Wu, et al.Human Genetics|May 28, 2004
Increased amount of the angiotensin-converting enzyme (ACE) mRNA originating from the ACE allele with deletionTadashi Suehiro, Tatsuhito Morita, Mari Inoue, et al.Human Genetics|September 1, 2005
Polymorphisms of complement receptor 1 and interleukin-10 genes and systemic lupus erythematosus: a meta-analysisSwapan K Nath, John B Harley, Young Ho LeeHuman Genetics|September 1, 2005
Familial aggregation in lone atrial fibrillationPatrick T Ellinor, Danita M Yoerger, Jeremy N Ruskin, et al.Human Genetics|September 1, 2005
The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decayL W Harries, Coralie Bingham, Christine Bellanne-Chantelot, et al.Human Genetics|September 1, 2005
Meprin beta metalloprotease gene polymorphisms associated with diabetic nephropathy in the Pima IndiansAlexander R Red Eagle, Robert L Hanson, Weiping Jiang, et al.Human Genetics|September 1, 2005
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohortHaiying Meng, Karl Hager, Matthew Held, et al.Human Genetics|September 1, 2005
Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 geneJens Michael Hertz, Ulf Persson, Inger Juncker, et al.Pageof 957