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Human Genetics|October 7, 2005
An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3' haplotypes could modify circulating levels of mannose-binding lectinToralf Bernig, Willemijn Breunis, Nannette Brouwer, et al.Human Genetics|March 4, 2005
A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotypeJérôme Clain, Jacqueline Lehmann-Che, Emmanuelle Girodon, et al.Human Genetics|May 1, 1992
Differential termination of primer extension: a novel, quantifiable method for detection of point mutationsD J Picketts, C Cameron, S A Taylor, et al.Human Genetics|May 1, 1992
Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: application to family studies in von Willebrand diseaseA M Cumming, J G Armstrong, K Pendry, et al.Human Genetics|May 1, 1992
Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youthS O'Rahilly, P Patel, O J Lehmann, et al.Human Genetics|November 13, 2004
Novel and recurrent mutations in the laminin-5 genes causing lethal junctional epidermolysis bullosa: molecular basis and clinical course of Herlitz diseaseChristiane Mühle, Qiu-Jie Jiang, Alexandra Charlesworth, et al.Human Genetics|December 4, 2004
Variation in meiotic recombination frequencies among human malesFei Sun, Kiril Trpkov, Alfred Rademaker, et al.Human Genetics|November 19, 2004
Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locusAnnika Rökman, Agnes B Baffoe-Bonnie, Elizabeth Gillanders, et al.Human Genetics|November 19, 2004
Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2AKazuki Kijima, Chikahiko Numakura, Hiroko Izumino, et al.Pageof 957