Works matching IS 03406717 AND DT 2010 AND VI 128 AND IP 4
Results: 14
Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 401, doi. 10.1007/s00439-010-0863-y
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- Publication type:
- Article
S.J.L. Knight: Monographs in Human Genetics, Vol. 18, Genetics of Mental Retardation.
- Published in:
- 2010
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- Publication type:
- Book Review
A homozygous mutation in LTBP2 causes isolated microspherophakia.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 365, doi. 10.1007/s00439-010-0858-8
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- Publication type:
- Article
Breakpoint determination of 15 large deletions in Peutz–Jeghers subjects.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 373, doi. 10.1007/s00439-010-0859-7
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- Publication type:
- Article
Allele-specific recognition of the 3′ splice site of INS intron 1.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 383, doi. 10.1007/s00439-010-0860-1
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- Publication type:
- Article
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 411, doi. 10.1007/s00439-010-0864-x
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- Publication type:
- Article
A biopsy sample reduction approach to identify significant alterations of the testicular transcriptome in the presence of Y-chromosomal microdeletions that are independent of germ cell composition.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 421, doi. 10.1007/s00439-010-0865-9
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- Publication type:
- Article
Walther W., Stein U.S. (eds): Gene therapy of cancer: methods and protocols, 2nd ed.
- Published in:
- 2010
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- Publication type:
- Book Review
An approach based on a genome-wide association study reveals candidate loci for narcolepsy.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 433, doi. 10.1007/s00439-010-0862-z
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- Publication type:
- Article
Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 453, doi. 10.1007/s00439-010-0873-9
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- Publication type:
- Article
Achalasia: will genetic studies provide insights?
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 353, doi. 10.1007/s00439-010-0874-8
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- Publication type:
- Article
Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33.
- Published in:
- 2010
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- Publication type:
- Report
No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patients with m.11778G>A.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 465, doi. 10.1007/s00439-010-0875-7
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- Publication type:
- Article
Susceptibility to chronic thromboembolic pulmonary hypertension may be conferred by miR- 759 via its targeted interaction with polymorphic fibrinogen alpha gene.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 443, doi. 10.1007/s00439-010-0866-8
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- Publication type:
- Article