Works matching IS 03406717 AND DT 2007 AND VI 121 AND IP 5
Results: 18
Association of ALOX5AP with ischemic stroke: a population-based case-control study.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 601, doi. 10.1007/s00439-007-0338-y
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- Publication type:
- Article
Genetic ancestry, population sub-structure, and cardiovascular disease-related traits among African-American participants in the CARDIA Study.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 565, doi. 10.1007/s00439-007-0350-2
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- Publication type:
- Article
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP).
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 577, doi. 10.1007/s00439-007-0349-8
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- Publication type:
- Article
Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 591, doi. 10.1007/s00439-007-0341-3
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- Publication type:
- Article
PGC-1α Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 609, doi. 10.1007/s00439-007-0352-0
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- Publication type:
- Article
Genetic admixture, adipocytokines, and adiposity in Black Americans: the Health, Aging, and Body Composition study.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 615, doi. 10.1007/s00439-007-0353-z
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- Publication type:
- Article
A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 625, doi. 10.1007/s00439-007-0354-y
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- Publication type:
- Article
A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 631, doi. 10.1007/s00439-007-0356-9
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- Publication type:
- Article
Genetic markers for glutamic acid decarboxylase do not predict insulin-dependent diabetes mellitus in pairs of affected siblings.
- Published in:
- 2007
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- Publication type:
- Correction Notice
Kenneth Lyons Jones (ed): Smith’s recognizable patterns of human malformation.
- Published in:
- 2007
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- Publication type:
- Book Review
J. R. Lupski and P.T. Stankiewicz: Genomic disorders: the genomic basis of disease.
- Published in:
- 2007
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- Publication type:
- Book Review
Anthony H. Futerman, Ari Zimran: Gaucher Disease.
- Published in:
- 2007
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- Publication type:
- Book Review
Genetic polymorphisms in transforming growth factor beta-1 (TGFB1) and childhood asthma and atopy.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 529, doi. 10.1007/s00439-007-0337-z
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- Publication type:
- Article
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 539, doi. 10.1007/s00439-007-0343-1
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- Publication type:
- Article
Testing for association based on excess allele sharing in a sample of related cases and controls.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 549, doi. 10.1007/s00439-007-0345-z
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- Publication type:
- Article
The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 635, doi. 10.1007/s00439-007-0361-z
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- Publication type:
- Article
Novel human pathological mutations.
- Published in:
- 2007
- Publication type:
- Erratum
A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36.
- Published in:
- Human Genetics, 2007, v. 121, n. 5, p. 559, doi. 10.1007/s00439-007-0348-9
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- Publication type:
- Article