Works matching IS 10184813 AND DT 2007 AND VI 15 AND IP 9
Results: 14
Support for involvement of the AHI1 locus in schizophrenia.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 988, doi. 10.1038/sj.ejhg.5201848
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- Article
ALOX5AP gene variants and risk of coronary artery disease: an angiography-based study.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 959, doi. 10.1038/sj.ejhg.5201854
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- Article
No association of ERCC1 C8092A and T19007C polymorphisms to cancer risk: a meta-analysis.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 967, doi. 10.1038/sj.ejhg.5201855
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The MRE11/RAD50/NBS1 complex destabilization in Lynch-syndrome patients.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 922, doi. 10.1038/sj.ejhg.5201858
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Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype–phenotype correlations.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 943, doi. 10.1038/sj.ejhg.5201859
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Homozygosity for a FBN1 missense mutation: clinical and molecular evidence for recessive Marfan syndrome.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 930, doi. 10.1038/sj.ejhg.5201865
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Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 974, doi. 10.1038/sj.ejhg.5201866
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- Article
How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 917, doi. 10.1038/sj.ejhg.5201867
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- Article
Linkage disequilibrium analysis of two genes mapping on OFC3: PVR and PVRL2.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 992, doi. 10.1038/sj.ejhg.5201868
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Population genetics of familial Mediterranean fever: a review.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 911, doi. 10.1038/sj.ejhg.5201869
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A comprehensive screen for SNP associations on chromosome region 5q31–33 in Swedish/Norwegian celiac disease families.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 980, doi. 10.1038/sj.ejhg.5201870
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- Article
Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRα reveals rare variants in diaphragmatic hernia patients.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 950, doi. 10.1038/sj.ejhg.5201872
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- Article
Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor (SPINK1) gene.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 936, doi. 10.1038/sj.ejhg.5201873
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Genetics of the ECG: QT or not QT- A genetic analysis of a complex electrophysiological trait confirms several previously detected associations.
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- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 909, doi. 10.1038/sj.ejhg.5201877
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- Article