Works matching IS 1434-5161 AND VI 51 AND IP 11 AND DT 2006
Results: 16
A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 1030, doi. 10.1007/s10038-006-0049-6
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Further investigations of glucose-6-phosphate dehydrogenase variants in Flores Island, eastern Indonesia.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 952, doi. 10.1007/s10038-006-0044-y
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β<sub>2</sub>-adrenergic receptor polymorphisms are associated with asthma and COPD in adults.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 943, doi. 10.1007/s10038-006-0043-z
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Four novel and three recurrent mutations of the BTK gene and pathogenic effects of putative splice mutations.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 1006, doi. 10.1007/s10038-006-0052-y
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GGN repeat length and GGN/CAG haplotype variations in the androgen receptor gene and prostate cancer risk in south Indian men.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 998, doi. 10.1007/s10038-006-0051-z
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The genetic and molecular basis of muscular dystrophy: roles of cell–matrix linkage in the pathogenesis.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 915, doi. 10.1007/s10038-006-0056-7
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Polymorphisms of the CD14 gene and atopic phenotypes in Czech patients with IgE-mediated allergy.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 977, doi. 10.1007/s10038-006-0050-0
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Prediction of systemic exposure to cyclosporine in Japanese pediatric patients.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 969, doi. 10.1007/s10038-006-0048-7
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Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 958, doi. 10.1007/s10038-006-0045-x
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Genetic structural differences between responders and non-responders to interferon therapy for chronic hepatitis-B patients.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 984, doi. 10.1007/s10038-006-0067-4
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Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searches.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 1015, doi. 10.1007/s10038-006-0053-x
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Association of estrogen receptor alpha gene polymorphisms and lifestyle factors with calcaneal quantitative ultrasound and osteoporosis in postmenopausal Vietnamese women.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 1022, doi. 10.1007/s10038-006-0055-8
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Molecular analysis of two uncharacterized sequence variants of the VHL gene.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 964, doi. 10.1007/s10038-006-0054-9
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A polymorphism of C-to-T substitution at −31 IL1B is associated with the risk of advanced gastric adenocarcinoma in a Japanese population.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 927, doi. 10.1007/s10038-006-0040-2
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New splicing mutations in propionic acidemia.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 992, doi. 10.1007/s10038-006-0068-3
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Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profiles.
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- Journal of Human Genetics, 2006, v. 51, n. 11, p. 934, doi. 10.1007/s10038-006-0042-0
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- Article