Works matching IS 03406717 AND DT 2010 AND VI 128 AND IP 2
Results: 12
Identification of HAVCR1 gene haplotypes associated with mRNA expression levels and susceptibility to autoimmune diseases.
- Published in:
- Human Genetics, 2010, v. 128, n. 2, p. 221, doi. 10.1007/s00439-010-0844-1
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- Publication type:
- Article
Association between genome-wide association studies reported SNPs and pediatric-onset Crohn’s disease in Canadian children.
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- Human Genetics, 2010, v. 128, n. 2, p. 131, doi. 10.1007/s00439-010-0835-2
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- Publication type:
- Article
The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression.
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- Human Genetics, 2010, v. 128, n. 2, p. 205, doi. 10.1007/s00439-010-0843-2
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- Article
Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population.
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- Human Genetics, 2010, v. 128, n. 2, p. 137, doi. 10.1007/s00439-010-0834-3
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- Publication type:
- Article
Genome-wide analysis of the structure of the South African Coloured Population in the Western Cape.
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- Human Genetics, 2010, v. 128, n. 2, p. 145, doi. 10.1007/s00439-010-0836-1
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- Publication type:
- Article
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs, David J. Weatherall: Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management.
- Published in:
- 2010
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- Publication type:
- Book Review
Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study.
- Published in:
- Human Genetics, 2010, v. 128, n. 2, p. 165, doi. 10.1007/s00439-010-0841-4
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- Publication type:
- Article
A locus for juvenile myoclonic epilepsy maps to 2q33–q36.
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- Human Genetics, 2010, v. 128, n. 2, p. 123, doi. 10.1007/s00439-010-0831-6
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- Publication type:
- Article
Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.
- Published in:
- Human Genetics, 2010, v. 128, n. 2, p. 179, doi. 10.1007/s00439-010-0837-0
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- Publication type:
- Article
Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.
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- Human Genetics, 2010, v. 128, n. 2, p. 195, doi. 10.1007/s00439-010-0842-3
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- Publication type:
- Article
Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes.
- Published in:
- Human Genetics, 2010, v. 128, n. 2, p. 213, doi. 10.1007/s00439-010-0847-y
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- Publication type:
- Article
Genetic determinants of autism in individuals with deletions of 18q.
- Published in:
- Human Genetics, 2010, v. 128, n. 2, p. 155, doi. 10.1007/s00439-010-0839-y
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- Publication type:
- Article