Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 3
Results: 12
A case–control association analysis of CABIN1 with schizophrenia in a Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 179, doi. 10.1038/jhg.2009.136
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- Article
Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 133, doi. 10.1038/jhg.2009.139
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- Article
Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 137, doi. 10.1038/jhg.2009.140
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- Article
Novel mutations in the SIL1 gene in a Japanese pedigree with the Marinesco–Sjögren syndrome.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 142, doi. 10.1038/jhg.2009.141
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- Article
Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 182, doi. 10.1038/jhg.2009.142
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- Article
Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 147, doi. 10.1038/jhg.2009.143
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- Article
A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 155, doi. 10.1038/jhg.2010.1
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- Article
A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen–Tawil syndrome.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 186, doi. 10.1038/jhg.2010.2
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- Article
Relationship between growth hormone 1 genetic polymorphism and susceptibility to colorectal cancer.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 163, doi. 10.1038/jhg.2010.3
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A functional polymorphism (−603A → G) in the tissue factor gene promoter is associated with adult-onset asthma.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 167, doi. 10.1038/jhg.2010.4
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Prediction of the clinical phenotype of Fabry disease based on protein sequential and structural information.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 175, doi. 10.1038/jhg.2010.5
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- Article
Identification of CYP19A1 single-nucleotide polymorphisms and their haplotype distributions in a Korean population.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 189, doi. 10.1038/jhg.2010.6
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- Article