Works matching IS 03406717 AND DT 2006 AND VI 120 AND IP 5
Results: 17
Identifying genes underlying skin pigmentation differences among human populations.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 613, doi. 10.1007/s00439-006-0256-4
- By:
- Publication type:
- Article
Localization and replication of the systemic lupus erythematosus linkage signal at 4p16: interaction with 2p11, 12q24 and 19q13 in European Americans.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 623, doi. 10.1007/s00439-006-0248-4
- By:
- Publication type:
- Article
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 663, doi. 10.1007/s00439-006-0237-7
- By:
- Publication type:
- Article
A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 653, doi. 10.1007/s00439-006-0246-6
- By:
- Publication type:
- Article
The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 633, doi. 10.1007/s00439-006-0249-3
- By:
- Publication type:
- Article
A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 737, doi. 10.1007/s00439-006-0241-y
- By:
- Publication type:
- Article
Lack of association between rs7566605 and obesity in a Chinese population.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Ian D. Young: Medical genetics.
- Published in:
- 2006
- By:
- Publication type:
- Book Review
Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 671, doi. 10.1007/s00439-006-0236-8
- By:
- Publication type:
- Article
Elevated male European and female African contributions to the genomes of African American individuals.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 713, doi. 10.1007/s00439-006-0261-7
- By:
- Publication type:
- Article
Predictors of uptake of obesity genetic testing among affected adults.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 641, doi. 10.1007/s00439-006-0252-8
- By:
- Publication type:
- Article
Association of Hck genetic polymorphisms with gene expression and COPD.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 681, doi. 10.1007/s00439-006-0253-7
- By:
- Publication type:
- Article
High-resolution mapping of DNA methylation in human genome using oligonucleotide tiling array.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 701, doi. 10.1007/s00439-006-0254-6
- By:
- Publication type:
- Article
Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 691, doi. 10.1007/s00439-006-0255-5
- By:
- Publication type:
- Article
Genetics of preeclampsia: paradigm shifts.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 607, doi. 10.1007/s00439-006-0259-1
- By:
- Publication type:
- Article
Fibrillin I gene polymorphism is associated with tall stature of normal individuals.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 733, doi. 10.1007/s00439-006-0263-5
- By:
- Publication type:
- Article
Paul Polani and the development of medical genetics.
- Published in:
- 2006
- By:
- Publication type:
- Editorial