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Annals of Human Genetics|May 28, 2009
High-resolution melting facilitates mutation screening of PYGM in patients with McArdle diseaseMorten Duno, Ros Quinlivan, John Vissing, et al.Annals of Human Genetics|May 30, 2009
First genetic insight into Libyan Tuaregs: a maternal perspectiveClaudio Ottoni, Cristina Martínez-Labarga, Eva-Liis Loogväli, et al.Annals of Human Genetics|May 1, 1991
Genetic similarity maps and immunoglobulin allotypes of eleven populations from the Pyrenees (France)S Hazout, J M Dugoujon, F Loirat, et al.Annals of Human Genetics|May 1, 1991
A new genetic polymorphism in human platelet polypeptides detected by two-dimensional electrophoresisE Kajii, S Iwamoto, T Omi, et al.Annals of Human Genetics|December 5, 2008
The complex and diversified mitochondrial gene pool of Berber populationsC Coudray, A Olivieri, A Achilli, et al.Annals of Human Genetics|January 13, 2009
Heterogeneous disease modeling for Hardy-Weinberg disequilibrium in case-control studies: application to renal stones and calcium-sensing receptor polymorphismsD C Hamilton, V K Grover, C A Smith, et al.Annals of Human Genetics|November 25, 2010
An alternative model for quantitative trait loci (QTL) analysis in general pedigreesSaonli Basu, James S PankowAnnals of Human Genetics|November 25, 2010
Bayesian models for detecting epistatic interactions from genetic dataYu Zhang, Bo Jiang, Jun Zhu, et al.Annals of Human Genetics|December 2, 2010
Importance measures for epistatic interactions in case-parent triosHolger Schwender, Katherine Bowers, M Daniele Fallin, et al.Annals of Human Genetics|April 5, 2013
Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohortLinlu Zhao, Michael B Bracken, Andrew T DeWanPageof 231