Works matching IS 03406717 AND DT 2003 AND VI 113 AND IP 5
Results: 15
Nicholas T. Potter (editor) Methods in molecular biology, volume 217. Neurogenetics: methods and protocols: Humana Press, ISBN 0-89603-990-0, hardcover (2002).
- Published in:
- 2003
- By:
- Publication type:
- Book Review
Association of a promoter variant in the inducible cyclooxygenase-2 gene (PTGS2) with type 2 diabetes mellitus in Pima Indians.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 377, doi. 10.1007/s00439-003-1000-y
- By:
- Publication type:
- Article
A common IL-13 Arg130Gln single nucleotide polymorphism among Chinese atopy patients with allergic rhinitis.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 387, doi. 10.1007/s00439-003-1001-x
- By:
- Publication type:
- Article
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 461, doi. 10.1007/s00439-003-1003-8
- By:
- Publication type:
- Article
Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 437, doi. 10.1007/s00439-003-1005-6
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- Publication type:
- Article
Mutations.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 465, doi. 10.1007/s00439-003-1014-5
- Publication type:
- Article
Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 426, doi. 10.1007/s00439-003-1002-9
- By:
- Publication type:
- Article
Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12).
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 447, doi. 10.1007/s00439-003-0981-x
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- Publication type:
- Article
Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 391, doi. 10.1007/s00439-003-1004-7
- By:
- Publication type:
- Article
Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 371, doi. 10.1007/s00439-003-0982-9
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- Publication type:
- Article
Molecular variation at the apolipoprotein B gene locus in relation to lipids and cardiovascular disease: a systematic meta-analysis.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 417, doi. 10.1007/s00439-003-0988-3
- By:
- Publication type:
- Article
Novel mutations in the IRF6 gene for Van der Woude syndrome.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 382, doi. 10.1007/s00439-003-0989-2
- By:
- Publication type:
- Article
Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 406, doi. 10.1007/s00439-003-0992-7
- By:
- Publication type:
- Article
Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 432, doi. 10.1007/s00439-003-0983-8
- By:
- Publication type:
- Article
Inherited BRCA2 mutations in African Americans with breast and/or ovarian cancer: a study of familial and early onset cases.
- Published in:
- Human Genetics, 2003, v. 113, n. 5, p. 452, doi. 10.1007/s00439-003-0999-0
- By:
- Publication type:
- Article