Works matching IS 10184813 AND DT 2005 AND VI 13 AND IP 7
Results: 19
Association between SLC11A1 (formerly NRAMP1) and the risk of sarcoidosis in Poland.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 829, doi. 10.1038/sj.ejhg.5201370
- By:
- Publication type:
- Article
Genetic stratification of pathogen-response-related and other variants within a homogeneous Caucasian Irish population.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 798, doi. 10.1038/sj.ejhg.5201382
- By:
- Publication type:
- Article
Hardy–Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations, and power.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 840, doi. 10.1038/sj.ejhg.5201410
- By:
- Publication type:
- Article
Hereditary hearing loss—the updated resource book more needed than ever.
- Published in:
- 2005
- By:
- Publication type:
- Book Review
Genetic Epidemiology.
- Published in:
- 2005
- By:
- Publication type:
- Book Review
Association of DLG5 R30Q variant with inflammatory bowel disease.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 835, doi. 10.1038/sj.ejhg.5201403
- By:
- Publication type:
- Article
Contrasting patterns of Y chromosome and mtDNA variation in Africa: evidence for sex-biased demographic processes.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 867, doi. 10.1038/sj.ejhg.5201408
- By:
- Publication type:
- Article
High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 856, doi. 10.1038/sj.ejhg.5201390
- By:
- Publication type:
- Article
Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 849, doi. 10.1038/sj.ejhg.5201413
- By:
- Publication type:
- Article
Genetic nephrology.
- Published in:
- 2005
- By:
- Publication type:
- Book Review
A classic genetic text about classic genetic texts.
- Published in:
- 2005
- By:
- Publication type:
- Book Review
An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 807, doi. 10.1038/sj.ejhg.5201418
- By:
- Publication type:
- Article
Childhood overgrowth in patients with common NF1 microdeletions.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 883, doi. 10.1038/sj.ejhg.5201419
- By:
- Publication type:
- Article
An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 815, doi. 10.1038/sj.ejhg.5201422
- By:
- Publication type:
- Article
Association of the CTLA-4 gene with rheumatoid arthritis in Chinese Han population.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 823, doi. 10.1038/sj.ejhg.5201423
- By:
- Publication type:
- Article
TaqIB polymorphism in CETP gene: the influence on incidence of cardiovascular disease in statin-treated patients with familial hypercholesterolemia.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 877, doi. 10.1038/sj.ejhg.5201426
- By:
- Publication type:
- Article
Complex Disease: A new vision for age-related macular degeneration.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 793, doi. 10.1038/sj.ejhg.5201431
- By:
- Publication type:
- Article
Immunogenetics: Safety in numbers.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 795, doi. 10.1038/sj.ejhg.5201434
- By:
- Publication type:
- Article
X Chromosome Inactivation: No longer ‘all-or-none’.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 7, p. 796, doi. 10.1038/sj.ejhg.5201443
- By:
- Publication type:
- Article