Works matching IS 10184813 AND DT 2005 AND VI 13 AND IP 12
Results: 11
Analysis of four neuroligin genes as candidates for autism.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1285, doi. 10.1038/sj.ejhg.5201474
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- Publication type:
- Article
Mutation spectrum leading to an attenuated phenotype in dystrophinopathies.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1254, doi. 10.1038/sj.ejhg.5201478
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- Publication type:
- Article
The place of the Basques in the European Y-chromosome diversity landscape.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1293, doi. 10.1038/sj.ejhg.5201482
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- Article
Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1275, doi. 10.1038/sj.ejhg.5201491
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- Publication type:
- Article
Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1268, doi. 10.1038/sj.ejhg.5201492
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- Publication type:
- Article
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1261, doi. 10.1038/sj.ejhg.5201493
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- Publication type:
- Article
Incidence of microduplication 22q11.2 in patients referred for FISH testing for velo cardiofacial and DiGeorge syndromes.
- Published in:
- 2005
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- Publication type:
- Letter
Molecular diagnosis of human cancer type by gene expression profiles and independent component analysis.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1303, doi. 10.1038/sj.ejhg.5201495
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- Publication type:
- Article
Management of hereditary dyslipidaemia; the paradigm of autosomal dominant hypercholesterolaemia.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1247, doi. 10.1038/sj.ejhg.5201496
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- Publication type:
- Article
Myotonic dystrophy-time to improve patient care and prepare for pathogenesis based treatments.
- Published in:
- 2005
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- Publication type:
- Book Review
Complex disease: Pleiotropic gene effects in obesity and type 2 diabetes.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1243, doi. 10.1038/sj.ejhg.5201514
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- Publication type:
- Article