Works matching IS 14345161 AND DT 2005 AND VI 50 AND IP 9
Results: 10
Glucose-6-phosphate dehydrogenase (G6PD) mutations in Cambodia: G6PD Viangchan (871G>A) is the most common variant in the Cambodian population.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 468, doi. 10.1007/s10038-005-0279-z
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- Article
Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in Jordan.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 435, doi. 10.1007/s10038-005-0274-4
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Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 490, doi. 10.1007/s10038-005-0283-3
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- Article
Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 473, doi. 10.1007/s10038-005-0280-6
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- Article
G6PD Viangchan (871G>A) is the most common G6PD-deficient variant in the Cambodian population.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 448, doi. 10.1007/s10038-005-0276-2
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- Article
A model of prediction system for adverse cardiovascular reactions by calcineurin inhibitors among patients with renal transplants using gene-based single-nucleotide polymorphisms.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 442, doi. 10.1007/s10038-005-0275-3
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- Article
Estrogen receptor α gene relationship with peak bone mass and body mass index in Chinese nuclear families.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 477, doi. 10.1007/s10038-005-0281-5
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- Article
Eosinophil infiltration in three patients with generalized atrophic benign epidermolysis bullosa from a Japanese family: molecular genetic and immunohistochemical studies.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 483, doi. 10.1007/s10038-005-0282-4
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- Article
Ankylosing spondylitis susceptibility loci defined by genome-search meta-analysis.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 453, doi. 10.1007/s10038-005-0277-1
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- Article
Establishment of immortalized Schwann cells from Sandhoff mice and corrective effect of recombinant human β-hexosaminidase A on the accumulated GM2 ganglioside.
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- Journal of Human Genetics, 2005, v. 50, n. 9, p. 460, doi. 10.1007/s10038-005-0278-0
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- Article