Works matching IS 10184813 AND DT 2008 AND VI 16 AND IP 5
Results: 21
Searching for genes influencing a complex disease: the case of coeliac disease.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 542, doi. 10.1038/sj.ejhg.5201918
- By:
- Publication type:
- Article
Warfarin Pharmacogenomics: A big step forward for individualized medicine: enlightened dosing of warfarin.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 532, doi. 10.1038/sj.ejhg.5201945
- By:
- Publication type:
- Article
Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 619, doi. 10.1038/sj.ejhg.5201996
- By:
- Publication type:
- Article
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach.
- Published in:
- 2008
- By:
- Publication type:
- Erratum
The VNTR 2 repeat in MAOA and delinquent behavior in adolescence and young adulthood: associations and MAOA promoter activity.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 626, doi. 10.1038/sj.ejhg.5201999
- By:
- Publication type:
- Article
A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 593, doi. 10.1038/sj.ejhg.5202000
- By:
- Publication type:
- Article
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 565, doi. 10.1038/sj.ejhg.5202001
- By:
- Publication type:
- Article
Evaluation of coverage variation of SNP chips for genome-wide association studies.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 635, doi. 10.1038/sj.ejhg.5202007
- By:
- Publication type:
- Article
The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 603, doi. 10.1038/sj.ejhg.5202003
- By:
- Publication type:
- Article
Composite measure of linkage disequilibrium for testing interaction between unlinked loci.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 644, doi. 10.1038/sj.ejhg.5202004
- By:
- Publication type:
- Article
Sporadic mutations in melanocortin receptor 3 in morbid obese individuals.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 581, doi. 10.1038/sj.ejhg.5202005
- By:
- Publication type:
- Article
Familial deletion within NLGN4 associated with autism and Tourette syndrome.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 614, doi. 10.1038/sj.ejhg.5202006
- By:
- Publication type:
- Article
Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 572, doi. 10.1038/sj.ejhg.5202002
- By:
- Publication type:
- Article
HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 652, doi. 10.1038/sj.ejhg.5202008
- By:
- Publication type:
- Article
Smith–Lemli–Opitz syndrome: pathogenesis, diagnosis and management.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 535, doi. 10.1038/ejhg.2008.10
- By:
- Publication type:
- Article
The success of the genome-wide association approach: a brief story of a long struggle.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 554, doi. 10.1038/ejhg.2008.12
- By:
- Publication type:
- Article
Memories from our genes: Genes, Culture, and Human Evolution: A Synthesis.
- Published in:
- 2008
- By:
- Publication type:
- Book Review
Linkage and association analysis of CACNG3 in childhood absence epilepsy.
- Published in:
- 2008
- By:
- Publication type:
- Erratum
Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice
Modifier Genes and HNPCC: Variable phenotypic expression in HNPCC and the search for modifier genes.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 531, doi. 10.1038/ejhg.2008.46
- By:
- Publication type:
- Article
No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 5, p. 587, doi. 10.1038/ejhg.2008.26
- By:
- Publication type:
- Article