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Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations.
Vergult, Sarah; Van Binsbergen, Ellen; Sante, Tom; Nowak, Silke; Vanakker, Olivier; Claes, Kathleen; Poppe, Bruce; Van der Aa, Nathalie; van Roosmalen, Markus J; Duran, Karen; Tavakoli-Yaraki, Masoumeh; Swinkels, Marielle; van den Boogaard, Marie-José; van Haelst, Mieke; Roelens, Filip; Speleman, Frank; Cuppen, Edwin; Mortier, Geert; Kloosterman, Wigard P; Menten, Björn.
Afiliação
  • Vergult S; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Van Binsbergen E; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Sante T; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Nowak S; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Vanakker O; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Claes K; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Poppe B; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Van der Aa N; Department for Medical Genetics, University Hospital of Antwerp, Antwerp, Belgium.
  • van Roosmalen MJ; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Duran K; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Tavakoli-Yaraki M; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Swinkels M; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van den Boogaard MJ; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Haelst M; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Roelens F; Heilig Hart Ziekenhuis, Roeselare, Belgium.
  • Speleman F; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Cuppen E; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Mortier G; 1] Center for Medical Genetics, Ghent University, Ghent, Belgium [2] Department for Medical Genetics, University Hospital of Antwerp, Antwerp, Belgium.
  • Kloosterman WP; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Menten B; Center for Medical Genetics, Ghent University, Ghent, Belgium.
Eur J Hum Genet ; 22(5): 652-9, 2014 May.
Article em En | MEDLINE | ID: mdl-24105367
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Aberrações Cromossômicas / Sequenciamento de Nucleotídeos em Larga Escala / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Bélgica País de publicação: Reino Unido
Texto completo
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XML
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Aberrações Cromossômicas / Sequenciamento de Nucleotídeos em Larga Escala / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Bélgica País de publicação: Reino Unido