Erratum to: Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging.
- Published in:
- 2010
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- Publication type:
- Correction Notice
Works matching IS 03406717 AND DT 2010 AND VI 127 AND IP 4
Results: 12
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Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 403, doi. 10.1007/s00439-009-0785-8
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- Publication type:
- Article
3
Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.
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- Human Genetics, 2010, v. 127, n. 4, p. 383, doi. 10.1007/s00439-009-0779-6
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- Publication type:
- Article
4
Michal Janitz (ed.) (2008): Next-Generation Genome Sequencing.
- Published in:
- 2010
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- Publication type:
- Book Review
5
Novel human pathological mutations.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 463, doi. 10.1007/s00439-010-0788-5
- Publication type:
- Article
6
Olby, Robert (2009): Francis Crick. Hunter of Life’s Secrets.
- Published in:
- 2010
- By:
- Publication type:
- Book Review
7
Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 441, doi. 10.1007/s00439-009-0782-y
- By:
- Publication type:
- Article
8
A genome-wide survey does not show the genetic distinctiveness of Basques.
- Published in:
- 2010
- By:
- Publication type:
- Report
9
Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 421, doi. 10.1007/s00439-009-0778-7
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- Publication type:
- Article
10
A meta-analysis of three polymorphisms in the endothelial nitric oxide synthase gene ( NOS3) and their effect on the risk of diabetic nephropathy.
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- Human Genetics, 2010, v. 127, n. 4, p. 373, doi. 10.1007/s00439-009-0783-x
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- Publication type:
- Article
11
Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 395, doi. 10.1007/s00439-009-0784-9
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- Publication type:
- Article
12
PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis.
- Published in:
- Human Genetics, 2010, v. 127, n. 4, p. 411, doi. 10.1007/s00439-009-0781-z
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- Publication type:
- Article