Found: 13
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Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 223, doi. 10.1007/s00439-009-0765-z
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- Publication type:
- Article
Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 125, doi. 10.1007/s00439-009-0767-x
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- Publication type:
- Article
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 155, doi. 10.1007/s00439-009-0754-2
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- Publication type:
- Article
Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
- Published in:
- 2010
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- Publication type:
- Correction Notice
Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 245, doi. 10.1007/s00439-009-0760-4
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- Publication type:
- Article
Transposable elements in disease-associated cryptic exons.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 135, doi. 10.1007/s00439-009-0752-4
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- Publication type:
- Article
Malaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypes.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 163, doi. 10.1007/s00439-009-0753-3
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- Publication type:
- Article
Common CFTR gene variants influence body composition and survival in rural Ghana.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 201, doi. 10.1007/s00439-009-0762-2
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- Publication type:
- Article
Genetic variation in PARL influences mitochondrial content.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 183, doi. 10.1007/s00439-009-0756-0
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- Publication type:
- Article
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 231, doi. 10.1007/s00439-009-0766-y
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- Publication type:
- Article
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 191, doi. 10.1007/s00439-009-0758-y
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- Publication type:
- Article
Rubella vaccine-induced cellular immunity: evidence of associations with polymorphisms in the Toll-like, vitamin A and D receptors, and innate immune response genes.
- Published in:
- Human Genetics, 2010, v. 127, n. 2, p. 207, doi. 10.1007/s00439-009-0763-1
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- Publication type:
- Article
R. C. Elston and W. D. Johnson: Basic biostatistics for geneticists and epidemiologists.
- Published in:
- 2010
- By:
- Publication type:
- Book Review