Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 1
Results: 22
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 123, doi. 10.1038/sj.ejhg.5201444
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- Article
A review of international and UK-based ethical guidelines for researchers conducting nontherapeutic genetic studies in developing countries.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 9, doi. 10.1038/sj.ejhg.5201497
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- Article
Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 85, doi. 10.1038/sj.ejhg.5201498
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- Article
Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 101, doi. 10.1038/sj.ejhg.5201499
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- Article
Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 34, doi. 10.1038/sj.ejhg.5201502
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- Article
Analysing DNA patents in relation with diagnostic genetic testing.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 26, doi. 10.1038/sj.ejhg.5201503
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- Article
Replication of IGF2-INS-TH<sup>*</sup>5 haplotype effect on obesity in older men and study of related phenotypes.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 109, doi. 10.1038/sj.ejhg.5201505
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- Article
Genetics of human heterotaxias.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 17, doi. 10.1038/sj.ejhg.5201506
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- Article
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 39, doi. 10.1038/sj.ejhg.5201507
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- Article
Evidence of genetic enrichment for exceptional survival using a family approach: the Leiden Longevity Study.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 79, doi. 10.1038/sj.ejhg.5201508
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- Article
Improving the accuracy of BRCA1/2 mutation prediction: validation of the novel country-customized IC software.
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- 2006
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- Publication type:
- Letter
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 127, doi. 10.1038/sj.ejhg.5201513
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- Article
Genetic background of HSH in three Polish families and a patient with an X;9 translocation.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 55, doi. 10.1038/sj.ejhg.5201515
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- Article
Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 63, doi. 10.1038/sj.ejhg.5201517
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- Article
Haplotype analysis of tumour necrosis factor receptor genes in 1p36: no evidence for association with systemic lupus erythematosus.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 69, doi. 10.1038/sj.ejhg.5201527
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Reply to Bottomley et al.
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- 2006
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- Publication type:
- Letter
Genome-wide linkage scan for spontaneous DZ twinning.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 117, doi. 10.1038/sj.ejhg.5201522
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Comment on ‘cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy’.
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- 2006
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- Publication type:
- Letter
Clock genes as a link between addiction and obesity.
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- 2006
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- Publication type:
- Letter
Cancer Transcriptomics: Modeling metastasis.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 1, doi. 10.1038/sj.ejhg.5201525
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- Article
Association of β<sub>2</sub> adrenergic receptor polymorphisms and related haplotypes with triglyceride and LDL-cholesterol levels.
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- 2006
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- Publication type:
- Letter
Mouse models: Psoriasis: an epidermal disease after all?
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 2, doi. 10.1038/sj.ejhg.5201543
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- Article