Works matching IS 14345161 AND DT 2008 AND VI 53 AND IP 8
Results: 12
Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 681, doi. 10.1007/s10038-008-0298-7
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Does increased nuchal translucency indicate a fetal abnormality? A retrospective study to clarify the clinical significance of nuchal translucency in Japan.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 688, doi. 10.1007/s10038-008-0299-6
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Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 694, doi. 10.1007/s10038-008-0300-4
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Reconstructing the origin of the Lapita Cultural Complex: mtDNA analyses of East Sepik Province, PNG.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 698, doi. 10.1007/s10038-008-0301-3
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The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 709, doi. 10.1007/s10038-008-0302-2
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Adiponectin gene ADIPOQ SNP associations with serum adiponectin in two female populations and effects of SNPs on promoter activity.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 718, doi. 10.1007/s10038-008-0303-1
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Association study of the C3 gene with adult and childhood asthma.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 728, doi. 10.1007/s10038-008-0304-0
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A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 764, doi. 10.1007/s10038-008-0305-z
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SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 769, doi. 10.1007/s10038-008-0306-y
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Two-stage designs to identify the effects of SNP combinations on complex diseases.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 739, doi. 10.1007/s10038-008-0307-x
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Grouping preprocess to accurately extend application of EM algorithm to haplotype inference.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 747, doi. 10.1007/s10038-008-0308-9
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- Article
Significant association of ABCG8:D19H gene polymorphism with hypercholesterolemia and insulin resistance.
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- Journal of Human Genetics, 2008, v. 53, n. 8, p. 757, doi. 10.1007/s10038-008-0310-2
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- Article