Novel human pathological mutations.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 101, doi. 10.1007/s00439-007-0461-9
- Publication type:
- Article
Works matching IS 03406717 AND DT 2008 AND VI 123 AND IP 1
Results: 13
1
2
Interaction between the UCP2–866G/A, mtDNA 10398G/A and PGC1α p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice
3
Association of rare chymotrypsinogen C ( CTRC) gene variations in patients with idiopathic chronic pancreatitis.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 83, doi. 10.1007/s00439-007-0459-3
- By:
- Publication type:
- Article
4
Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 65, doi. 10.1007/s00439-007-0451-y
- By:
- Publication type:
- Article
5
Promoter methylation study of the H37/RBM5 tumor suppressor gene from the 3p21.3 human lung cancer tumor suppressor locus.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 55, doi. 10.1007/s00439-007-0449-5
- By:
- Publication type:
- Article
6
A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 41, doi. 10.1007/s00439-007-0447-7
- By:
- Publication type:
- Article
7
Relationship between two sequence variations in the gene for peroxisome proliferator-activated receptor-gamma and plasma homocysteine concentration. Health in men study.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 35, doi. 10.1007/s00439-007-0446-8
- By:
- Publication type:
- Article
8
Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 93, doi. 10.1007/s00439-007-0444-x
- By:
- Publication type:
- Article
9
Methods for meta-analysis in genetic association studies: a review of their potential and pitfalls.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 1, doi. 10.1007/s00439-007-0445-9
- By:
- Publication type:
- Article
10
Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology?
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 15, doi. 10.1007/s00439-007-0448-6
- By:
- Publication type:
- Article
11
Comments on the entropy-based transmission/disequilibrium test.
- Published in:
- 2008
- By:
- Publication type:
- Letter
12
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2.
- Published in:
- Human Genetics, 2008, v. 123, n. 1, p. 77, doi. 10.1007/s00439-007-0452-x
- By:
- Publication type:
- Article
13
PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice