Works matching IS 14345161 AND DT 2009 AND VI 54 AND IP 11
Results: 12
Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 681, doi. 10.1038/jhg.2009.100
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- Article
Serotonin 1A receptor gene and major depressive disorder: an association study and meta-analysis.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 629, doi. 10.1038/jhg.2009.84
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- Article
pHCR: a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 634, doi. 10.1038/jhg.2009.85
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- Article
Validation of eight genetic risk factors in East Asian populations replicated the association of BRAP with coronary artery disease.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 642, doi. 10.1038/jhg.2009.87
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- Article
mtDNA G10398A variant in African-American women with breast cancer provides resistance to apoptosis and promotes metastasis in mice.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 647, doi. 10.1038/jhg.2009.89
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- Article
Polymorphisms and haplotypes in TLR9 and MYD88 are associated with the development of Hodgkin's lymphoma: a candidate–gene association study.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 655, doi. 10.1038/jhg.2009.90
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- Article
ACTA2 is not a major disease-causing gene for moyamoya disease.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 687, doi. 10.1038/jhg.2009.91
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- Article
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 660, doi. 10.1038/jhg.2009.92
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- Article
Thalamic transcriptome screening in three psychiatric states.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 665, doi. 10.1038/jhg.2009.93
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Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 615, doi. 10.1038/jhg.2009.95
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Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 676, doi. 10.1038/jhg.2009.96
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- Article
The era of genome-wide association studies: opportunities and challenges for asthma genetics.
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- Journal of Human Genetics, 2009, v. 54, n. 11, p. 624, doi. 10.1038/jhg.2009.97
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- Article