Works matching IS 03406717 AND DT 2011 AND VI 130 AND IP 6
Results: 13
A miRNA-492 binding-site polymorphism in BSG ( basigin) confers risk to psoriasis in Central South Chinese population.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 749, doi. 10.1007/s00439-011-1026-5
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- Publication type:
- Article
Alterations of ATM and CADM1 in chromosomal 11q22.3-23.2 region are associated with the development of invasive cervical carcinoma.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 735, doi. 10.1007/s00439-011-1015-8
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- Publication type:
- Article
A mutation screen in patients with Kabuki syndrome.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 715, doi. 10.1007/s00439-011-1004-y
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- Publication type:
- Article
Two-marker association tests yield new disease associations for coronary artery disease and hypertension.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 725, doi. 10.1007/s00439-011-1009-6
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- Publication type:
- Article
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 759, doi. 10.1007/s00439-011-1018-5
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- Publication type:
- Article
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer risk.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 767, doi. 10.1007/s00439-011-1025-6
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- Article
Anticipation in hereditary disease: the history of a biomedical concept.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 705, doi. 10.1007/s00439-011-1022-9
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- Publication type:
- Article
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 777, doi. 10.1007/s00439-011-1020-y
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- Publication type:
- Article
Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 789, doi. 10.1007/s00439-011-1039-0
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- Publication type:
- Article
Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 795, doi. 10.1007/s00439-011-1033-6
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- Publication type:
- Article
MHC region and risk of systemic lupus erythematosus in African American women.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 807, doi. 10.1007/s00439-011-1045-2
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- Publication type:
- Article
Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.
- Published in:
- Human Genetics, 2011, v. 130, n. 6, p. 817, doi. 10.1007/s00439-011-1041-6
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- Publication type:
- Article
John C. Avise: Inside the human genome: a case for non-intelligent design.
- Published in:
- 2011
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- Publication type:
- Book Review