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Human Genetics|June 5, 2007
Common genetic variation in eight genes of the GH/IGF1 axis does not contribute to adult height variationGuillaume Lettre, Johannah L Butler, Kristin G Ardlie, et al.Human Genetics|May 9, 2007
Bivariate linkage confirms genetic contribution to fetal origins of childhood growth and cardiovascular disease risk in Hispanic childrenGuowen Cai, Shelley A Cole, Karin Haack, et al.Human Genetics|May 12, 2007
Sex-specific effects of ACE I/D and AGT-M235T on pulse pressure: the HyperGEN StudyAmy I Lynch, Donna K Arnett, James S Pankow, et al.Human Genetics|July 3, 2007
A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3Sylvain Hanein, Alexandra Dürr, Pascale Ribai, et al.Human Genetics|July 5, 2007
Deletions in chromosome 4 differentially associated with the development of cervical cancer: evidence of slit2 as a candidate tumor suppressor geneRatnesh Kumar Singh, Dipanjana Indra, Sraboni Mitra, et al.Human Genetics|September 1, 1991
Chromosomal localization of the human D3 dopamine receptor geneM Le Coniat, P Sokoloff, J Hillion, et al.Human Genetics|February 3, 2009
Mutation screening of apical sodium-dependent bile acid transporter (SLC10A2): novel haplotype block including six newly identified variants linked to reduced expressionOlga Renner, Simone Harsch, Elke Schaeffeler, et al.Human Genetics|October 1, 1991
Cystic fibrosis allele frequency, sex ratio anomalies and fertility: a new theory for the dissemination of mutant allelesD J PritchardHuman Genetics|October 1, 1991
Cytogenetic and molecular characterization of a small ring chromosome in the complex karyotype of a girl with Turner syndromeM Guttenbach, J Köhler, M SchmidHuman Genetics|October 1, 1991
Information content of the Centre d'Etude du Polymorphisme Humain (CEPH) family structures for linkage studiesA ChakravartiPageof 958