Found: 13
Select item for more details and to access through your institution.
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
- By:
- Publication type:
- Article
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 59, doi. 10.1007/s00439-010-0899-z
- By:
- Publication type:
- Article
Regions of homozygosity and their impact on complex diseases and traits.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 1, doi. 10.1007/s00439-010-0920-6
- By:
- Publication type:
- Article
Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approach.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 35, doi. 10.1007/s00439-010-0894-4
- By:
- Publication type:
- Article
Heather Skirton and Christine Patch: Genetics for the health sciences: a handbook for clinical healthcare.
- Published in:
- 2011
- By:
- Publication type:
- Book Review
−13915*G DNA polymorphism associated with lactase persistence in Africa interacts with Oct-1.
- Published in:
- 2011
- By:
- 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
- By:
- Publication type:
- Article
Mutation analysis in Bardet-Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 79, doi. 10.1007/s00439-010-0902-8
- By:
- Publication type:
- 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
- By:
- 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
- By:
- Publication type:
- 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
- By:
- 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
- By:
- Publication type:
- Article
Mechanisms for phenotypic variation in Lesch-Nyhan disease and its variants.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 71, doi. 10.1007/s00439-010-0901-9
- By:
- Publication type:
- Article