Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 10
Results: 16
Tuberous sclerosis.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1065, doi. 10.1038/sj.ejhg.5201625
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- Publication type:
- Article
Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1074, doi. 10.1038/sj.ejhg.5201649
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- Publication type:
- Article
Reply to Hochstenbach et al.
- Published in:
- 2006
- By:
- Publication type:
- Letter
No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis.
- Published in:
- 2006
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- Publication type:
- Letter
Chromosome 5 and Parkinson disease.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1106, doi. 10.1038/sj.ejhg.5201666
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- Publication type:
- Article
The downstream modulator of interferon-γ, STAT1 is not genetically associated to the Dutch coeliac disease population.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1120, doi. 10.1038/sj.ejhg.5201667
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- Publication type:
- Article
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1097, doi. 10.1038/sj.ejhg.5201670
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- Publication type:
- Article
A breath of fresh air: Respiratory Genetics.
- Published in:
- 2006
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- Publication type:
- Book Review
Syndrome identification based on 2D analysis software.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1082, doi. 10.1038/sj.ejhg.5201673
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- Publication type:
- Article
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1090, doi. 10.1038/sj.ejhg.5201674
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- Publication type:
- Article
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1111, doi. 10.1038/sj.ejhg.5201675
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- Publication type:
- Article
Association of a 31 bp VNTR in the CBS gene with postload homocysteine concentrations in the Framingham Offspring Study.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1125, doi. 10.1038/sj.ejhg.5201677
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- Publication type:
- Article
A balanced perspective of psychiatric genetics: Psychiatric Genetics and Genomics.
- Published in:
- 2006
- By:
- Publication type:
- Book Review
Association study of the G-protein signaling 4 (RGS4) and proline dehydrogenase (PRODH) genes with schizophrenia: a meta-analysis.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1130, doi. 10.1038/sj.ejhg.5201680
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- Publication type:
- Article
DNA repair gene XRCC3 polymorphisms and cancer risk: a meta-analysis of 48 case–control studies.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1136, doi. 10.1038/sj.ejhg.5201681
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- Publication type:
- Article
Parkinson's Disease: The LRRK2-G2019S mutation: opening a novel era in Parkinson's disease genetics.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1061, doi. 10.1038/sj.ejhg.5201695
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- Publication type:
- Article