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Clinical Genetics|March 18, 2006
Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levelsS M Boekholdt, O W Souverein, M W T Tanck, et al.Clinical Genetics|March 18, 2006
Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemiaK Brusgaard, P Jordan, H Hansen, et al.Clinical Genetics|December 14, 2007
Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplicationS Yu, K Cox, K Friend, et al.Clinical Genetics|January 26, 2008
Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian PeninsulaM Mangas, C Nogueira, M J Prata, et al.Clinical Genetics|January 23, 1999
Inherited breast cancer: an emerging pictureP L Welcsh, E L Schubert, M C KingClinical Genetics|January 23, 1999
The long and the short of it: developmental genetics of the skeletal dysplasiasS D Dreyer, G Zhou, B LeeClinical Genetics|January 23, 1999
Predictive testing for Huntington's disease: II. Qualitative findings from a study of uptake in South WalesJ Binedell, J R Soldan, P S HarperClinical Genetics|January 23, 1999
Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitusR J Gardner, D O Robinson, L Lamont, et al.Clinical Genetics|February 16, 2002
Distribution of alpha1-antitrypsin PI S and PI Z frequencies in countries outside Europe: a meta-analysisI Blanco, E F Bustillo, M C RodriguezPageof 718