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Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.
van der Werf, Ilse M; Van Dijck, Anke; Reyniers, Edwin; Helsmoortel, Céline; Kumar, Ajay Anand; Kalscheuer, Vera M; de Brouwer, Arjan Pm; Kleefstra, Tjitske; van Bokhoven, Hans; Mortier, Geert; Janssens, Sandra; Vandeweyer, Geert; Kooy, R Frank.
Afiliação
  • van der Werf IM; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Van Dijck A; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Reyniers E; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Helsmoortel C; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Kumar AA; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Kalscheuer VM; Research Group Development and Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • de Brouwer AP; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Kleefstra T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Bokhoven H; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Mortier G; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Janssens S; Center for Medical Genetics Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.
  • Vandeweyer G; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.
  • Kooy RF; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium. Electronic address: Frank.Kooy@uantwerpen.be.
Gene ; 605: 92-98, 2017 Mar 20.
Article em En | MEDLINE | ID: mdl-27993705
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transtornos da Articulação / Predisposição Genética para Doença / Proteínas de Ligação a DNA / Genes Ligados ao Cromossomo X / Transtorno do Espectro Autista / Deficiência Intelectual / Mutação Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Gene Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Bélgica
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transtornos da Articulação / Predisposição Genética para Doença / Proteínas de Ligação a DNA / Genes Ligados ao Cromossomo X / Transtorno do Espectro Autista / Deficiência Intelectual / Mutação Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Gene Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Bélgica