Found: 11
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Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.
- Published in:
- Journal of Human Genetics, 2007, v. 52, n. 8, p. 643, doi. 10.1007/s10038-007-0154-1
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- Article
A grid-search algorithm for optimal allocation of sample size in two-stage association studies.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 650, doi. 10.1007/s10038-007-0159-9
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- Article
The association of Y chromosome haplogroups with spermatogenic failure in the Han Chinese.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 659, doi. 10.1007/s10038-007-0160-3
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- Article
Association of the aspartic acid-repeat polymorphism in the asporin gene with age at onset of knee osteoarthritis in Han Chinese Population.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 664, doi. 10.1007/s10038-007-0166-x
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- Article
Lack of association of fragile histidine triad ( FHIT) polymorphisms with lung cancer in the Korean population.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 668, doi. 10.1007/s10038-007-0169-7
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- Article
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 675, doi. 10.1007/s10038-007-0170-1
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- Article
Longevity-associated mitochondrial DNA 5178 C/A polymorphism and its interaction with cigarette consumption are associated with pulmonary function in middle-aged Japanese men.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 680, doi. 10.1007/s10038-007-0171-0
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- Article
A Japanese patient with a mild Lenz–Majewski syndrome.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 686, doi. 10.1007/s10038-007-0165-y
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- Article
OCA2*481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 690, doi. 10.1007/s10038-007-0167-9
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- Article
TP53 codon 72 polymorphism in 12 populations of insular Southeast Asia and Oceania.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 694, doi. 10.1007/s10038-007-0168-8
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- Article
Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.
- Published in:
- Journal of Human Genetics, 2007, v. 52, n. 8, p. 698, doi. 10.1007/s10038-007-0173-y
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- Article