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European Journal of Human Genetics : EJHG|May 10, 2007
The federated database--a basis for biobank-based post-genome studies, integrating phenome and genome data from 600,000 twin pairs in EuropeJuha Muilu, Leena Peltonen, Jan-Eric LittonEuropean Journal of Human Genetics : EJHG|May 10, 2007
Genetic influences on angina pectoris and its impact on coronary heart diseaseSlobodan Zdravkovic, Andreas Wienke, Nancy L Pedersen, et al.European Journal of Human Genetics : EJHG|May 10, 2007
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24Alessia Deglincerti, Roberto De Giorgio, Kivanc Cefle, et al.European Journal of Human Genetics : EJHG|February 10, 2007
Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autismDries Castermans, Joris R Vermeesch, Jean-Pierre Fryns, et al.European Journal of Human Genetics : EJHG|February 10, 2007
Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'Mylène Béri-Deixheimer, Marie-José Gregoire, Annick Toutain, et al.European Journal of Human Genetics : EJHG|February 10, 2007
Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literatureSiulan Vendramini, Antonio Richieri-Costa, Maria Leine Guion-AlmeidaEuropean Journal of Human Genetics : EJHG|May 25, 2007
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlationsTrilochan Sahoo, Carlos A Bacino, Jennifer R German, et al.European Journal of Human Genetics : EJHG|May 25, 2007
No association of ERCC1 C8092A and T19007C polymorphisms to cancer risk: a meta-analysisYuanchun Li, Shaohua Gu, Qihan Wu, et al.European Journal of Human Genetics : EJHG|November 30, 2006
Preselection of cases through expert clinical and radiological review significantly increases mutation detection rate in multiple epiphyseal dysplasiaAndreas Zankl, Gail C Jackson, Laureane Mittaz Crettol, et al.European Journal of Human Genetics : EJHG|May 31, 2007
How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing NetworkMark Kroese, Ron L Zimmern, Peter Farndon, et al.Pageof 564