Works matching IS 14345161 AND DT 2007 AND VI 52 AND IP 10
Results: 9
Novel and recurrent ALDH3A2 mutations in Italian patients with Sjögren–Larsson syndrome.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 865, doi. 10.1007/s10038-007-0180-z
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Genetic variations and haplotype structures of the DPYD gene encoding dihydropyrimidine dehydrogenase in Japanese and their ethnic differences.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 804, doi. 10.1007/s10038-007-0186-6
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Association analysis of HSP90B1 with bipolar disorder.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 794, doi. 10.1007/s10038-007-0188-4
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- Article
Role of genetic polymorphisms in ACE and TNF-α gene in sarcoidosis: a meta-analysis.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 836, doi. 10.1007/s10038-007-0185-7
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Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 820, doi. 10.1007/s10038-007-0187-5
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High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene ( GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 856, doi. 10.1007/s10038-007-0183-9
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Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 848, doi. 10.1007/s10038-007-0182-x
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- Article
SNPs in the KCNJ11- ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 781, doi. 10.1007/s10038-007-0190-x
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Danon disease presenting with dilated cardiomyopathy and a complex phenotype.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 830, doi. 10.1007/s10038-007-0184-8
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- Article