Works matching IS 03406717 AND DT 2010 AND VI 127 AND IP 6
Results: 15
Evidence for inheritance in patients with VACTERL association.
- Published in:
- 2010
- By:
- Publication type:
- Report
Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 691, doi. 10.1007/s00439-010-0818-3
- By:
- Publication type:
- Article
Malcolm Collins: Medicine and Sports Science, Vol. 54: Genetics and Sports.
- Published in:
- 2010
- By:
- Publication type:
- Book Review
Fine mapping of the 9q31 Hirschsprung’s disease locus.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 675, doi. 10.1007/s00439-010-0813-8
- By:
- Publication type:
- Article
Power analysis for case–control association studies of samples with known family histories.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 699, doi. 10.1007/s00439-010-0824-5
- By:
- Publication type:
- Article
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 705, doi. 10.1007/s00439-010-0819-2
- By:
- Publication type:
- Article
A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 721, doi. 10.1007/s00439-010-0820-9
- By:
- Publication type:
- Article
West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 629, doi. 10.1007/s00439-010-0803-x
- By:
- Publication type:
- Article
Philippe Collas (ed): Chromatin immunoprecipitation assays: methods and protocols.
- Published in:
- 2010
- By:
- Publication type:
- Book Review
Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 651, doi. 10.1007/s00439-010-0810-y
- By:
- Publication type:
- Article
Two-stage case–control designs for rare genetic variants.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 659, doi. 10.1007/s00439-010-0811-x
- By:
- Publication type:
- Article
Heritability of chronic venous disease.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 669, doi. 10.1007/s00439-010-0812-9
- By:
- Publication type:
- Article
Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 619, doi. 10.1007/s00439-010-0822-7
- By:
- Publication type:
- Article
Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 639, doi. 10.1007/s00439-010-0807-6
- By:
- Publication type:
- Article
A single nucleotide polymorphism in the FADS1/ FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyle.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 685, doi. 10.1007/s00439-010-0815-6
- By:
- Publication type:
- Article