Works matching IS 03406717 AND DT 2011 AND VI 129 AND IP 1
Results: 13
A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 45, doi. 10.1007/s00439-010-0896-2
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- Publication type:
- Article
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
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- Human Genetics, 2011, v. 129, n. 1, p. 59, doi. 10.1007/s00439-010-0899-z
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- Article
Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approach.
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- Human Genetics, 2011, v. 129, n. 1, p. 35, doi. 10.1007/s00439-010-0894-4
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- Article
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 51, doi. 10.1007/s00439-010-0897-1
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- Article
Mechanisms for phenotypic variation in Lesch-Nyhan disease and its variants.
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- Human Genetics, 2011, v. 129, n. 1, p. 71, doi. 10.1007/s00439-010-0901-9
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- Article
Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 25, doi. 10.1007/s00439-010-0893-5
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- Article
Heather Skirton and Christine Patch: Genetics for the health sciences: a handbook for clinical healthcare.
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- 2011
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- Publication type:
- Book Review
−13915*G DNA polymorphism associated with lactase persistence in Africa interacts with Oct-1.
- Published in:
- 2011
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- Publication type:
- Report
A novel survival multifactor dimensionality reduction method for detecting gene-gene interactions with application to bladder cancer prognosis.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 101, doi. 10.1007/s00439-010-0905-5
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- Publication type:
- Article
Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals.
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- Human Genetics, 2011, v. 129, n. 1, p. 79, doi. 10.1007/s00439-010-0902-8
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- Publication type:
- Article
Regions of homozygosity and their impact on complex diseases and traits.
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- Human Genetics, 2011, v. 129, n. 1, p. 1, doi. 10.1007/s00439-010-0920-6
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- Publication type:
- Article
Genetic variants in the KIF6 region and coronary event reduction from statin therapy.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 17, doi. 10.1007/s00439-010-0892-6
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- Publication type:
- Article
Genome-wide analysis of copy number variants in age-related macular degeneration.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 91, doi. 10.1007/s00439-010-0904-6
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- Publication type:
- Article