Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 10
Results: 14
Polymorphisms and allele frequencies of the ABO blood group gene among the Jomon, Epi-Jomon and Okhotsk people in Hokkaido, northern Japan, revealed by ancient DNA analysis.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 10, p. 691, doi. 10.1038/jhg.2010.90
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- Article
GATA transcription factors in congenital heart defects: A Commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.
- Published in:
- 2010
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- Publication type:
- Opinion
Association of polymorphisms in the RAGE gene with serum CRP levels and coronary artery disease in the Chinese Han population.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 10, p. 668, doi. 10.1038/jhg.2010.85
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- Article
Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 681, doi. 10.1038/jhg.2010.88
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- Article
A Commentary on genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.
- Published in:
- 2010
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- Publication type:
- Opinion
A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 662, doi. 10.1038/jhg.2010.84
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- Article
Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population: a case-control study.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 704, doi. 10.1038/jhg.2010.86
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- Article
Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 697, doi. 10.1038/jhg.2010.91
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- Publication type:
- Article
Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 656, doi. 10.1038/jhg.2010.82
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- Article
Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 649, doi. 10.1038/jhg.2010.79
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- Article
Analysis of LDLR mRNA in patients with familial hypercholesterolemia revealed a novel mutation in intron 14, which activates a cryptic splice site.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 10, p. 676, doi. 10.1038/jhg.2010.87
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- Article
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
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- Journal of Human Genetics, 2010, v. 55, n. 10, p. 639, doi. 10.1038/jhg.2010.96
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- Article
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 10, p. 701, doi. 10.1038/jhg.2010.83
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- Publication type:
- Article
Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 10, p. 707, doi. 10.1038/jhg.2010.92
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- Publication type:
- Article