Distribution of ITPA P32T alleles in multiple world populations.
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 10, p. 579, doi. 10.1007/s10038-004-0183-y
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- Publication type:
- Article
Works matching IS 14345161 AND DT 2004 AND VI 49 AND IP 10
Results: 10
1
2
Genetic analysis of the cardiac sodium channel geneSCN5Ain Koreans with Brugada syndrome.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 573, doi. 10.1007/s10038-004-0182-z
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- Article
3
Glucose-6-phosphate dehydrogenase (G6PD) mutations in Myanmar: G6PD Mahidol (487G>A) is the most common variant in the Myanmar population.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 544, doi. 10.1007/s10038-004-0187-7
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- Article
4
A frameshift variant of CYP2C8 was identified in a patient who suffered from rhabdomyolysis after administration of cerivastatin.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 582, doi. 10.1007/s10038-004-0188-6
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- Article
5
Interleukin 3 (IL3) polymorphisms associated with decreased risk of asthma and atopy.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 517, doi. 10.1007/s10038-004-0184-x
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- Article
6
Feasibility of gene therapy in Gaucher disease using an adeno-associated virus vector.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 536, doi. 10.1007/s10038-004-0186-8
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- Article
7
Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 558, doi. 10.1007/s10038-004-0190-z
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- Publication type:
- Article
8
Novel interferon regulatory factor-1 polymorphisms in a Kenyan population revealed by complete gene sequencing.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 528, doi. 10.1007/s10038-004-0185-9
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- Article
9
An insertion/deletionTEX28polymorphism and its application to analysis of red/green visual pigment gene arrays.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 548, doi. 10.1007/s10038-004-0189-5
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- Article
10
Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion ofSNF5/INI1in a newly established cell line derived from extrarenal rhabdoid tumor.
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 10, p. 586, doi. 10.1007/s10038-004-0191-y
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- Publication type:
- Article