Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 6
Results: 11
Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 518, doi. 10.1007/s10038-006-0392-7
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- Publication type:
- Article
Evolutionary dynamics of olfactory and other chemosensory receptor genes in vertebrates.
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- Journal of Human Genetics, 2006, v. 51, n. 6, p. 505, doi. 10.1007/s10038-006-0391-8
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- Publication type:
- Article
Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype–phenotype correlation.
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- Journal of Human Genetics, 2006, v. 51, n. 6, p. 548, doi. 10.1007/s10038-006-0396-3
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- Article
No evidence for association of the ENPP1 (PC-1) K121Q variant with risk of type 2 diabetes in a Japanese population.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 559, doi. 10.1007/s10038-006-0399-0
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- Article
Humanin expression in skeletal muscles of patients with chronic progressive external ophthalmoplegia.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 555, doi. 10.1007/s10038-006-0397-2
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- Article
Analyses of 5′ regulatory region polymorphisms in human SLC22A6 ( OAT1) and SLC22A8 ( OAT3).
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 575, doi. 10.1007/s10038-006-0398-1
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- Publication type:
- Article
Molecular cytogenetic characteristics of Down syndrome newborns.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 541, doi. 10.1007/s10038-006-0395-4
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- Publication type:
- Article
Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 533, doi. 10.1007/s10038-006-0394-5
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- Publication type:
- Article
A two-stage design for multiple testing in large-scale association studies.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 523, doi. 10.1007/s10038-006-0393-6
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- Article
A eulogy to the late Dr. Shiro Miwa.
- Published in:
- 2006
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- Publication type:
- Obituary
A common functional exon polymorphism in the microsomal triglyceride transfer protein gene is associated with type 2 diabetes, impaired glucose metabolism and insulin levels.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 6, p. 567, doi. 10.1007/s10038-006-0400-y
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- Article