Adaptive evolution of loci covarying with the human African Pygmy phenotype.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1305, doi. 10.1007/s00439-012-1157-3
- By:
- Publication type:
- Article
Works matching IS 03406717 AND DT 2012 AND VI 131 AND IP 8
Results: 10
1
2
Increased risk of stroke in oral contraceptive users carried replicated genetic variants: a population-based case-control study in China.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1337, doi. 10.1007/s00439-012-1161-7
- By:
- Publication type:
- Article
3
Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1295, doi. 10.1007/s00439-012-1156-4
- By:
- Publication type:
- Article
4
A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1319, doi. 10.1007/s00439-012-1158-2
- By:
- Publication type:
- Article
5
Using graded response model for the prediction of prostate cancer risk.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1327, doi. 10.1007/s00439-012-1160-8
- By:
- Publication type:
- Article
6
Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1345, doi. 10.1007/s00439-012-1165-3
- By:
- Publication type:
- Article
7
Further clarification of the contribution of the ADH1C gene to vulnerability of alcoholism and selected liver diseases.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1361, doi. 10.1007/s00439-012-1163-5
- By:
- Publication type:
- Article
8
McKinlay Gardner RJ, Sutherland GR, Shaffer LG: Chromosome abnormalities and genetic counselling.
- Published in:
- 2012
- By:
- Publication type:
- Book Review
9
Mouse models of SMA: tools for disease characterization and therapeutic development.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1277, doi. 10.1007/s00439-012-1171-5
- By:
- Publication type:
- Article
10
Reduced interferon (IFN)-α conditioned by IFNA2 (−173) and IFNA8 (−884) haplotypes is associated with enhanced susceptibility to severe malarial anemia and longitudinal all-cause mortality.
- Published in:
- Human Genetics, 2012, v. 131, n. 8, p. 1375, doi. 10.1007/s00439-012-1175-1
- By:
- Publication type:
- Article