Works matching IS 14345161 AND DT 2005 AND VI 50 AND IP 10
Results: 8
The Glu23Lys polymorphism in KCNJ11 and impaired hypoglycaemia awareness in patients with type 1 diabetes.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 530, doi. 10.1007/s10038-005-0288-y
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- Article
Androgenic correlates of genetic variation in the gene encoding 5α-reductase type 1.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 534, doi. 10.1007/s10038-005-0289-x
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- Article
Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 507, doi. 10.1007/s10038-005-0285-1
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Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 543, doi. 10.1007/s10038-005-0290-4
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- Article
Molecular characterization of Egyptian patients with glycogen storage disease type IIIa.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 538, doi. 10.1007/s10038-005-0291-3
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- Article
A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 523, doi. 10.1007/s10038-005-0287-z
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- Article
Refinement of the DFNA41 locus and candidate genes analysis.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 516, doi. 10.1007/s10038-005-0286-0
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- Article
Human mtDNA hypervariable regions, HVR I and II, hint at deep common maternal founder and subsequent maternal gene flow in Indian population groups.
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- Journal of Human Genetics, 2005, v. 50, n. 10, p. 497, doi. 10.1007/s10038-005-0284-2
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- Article