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Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder.
Lévy, Jonathan; Cogan, Guillaume; Maruani, Anna; Maillard, Arnaud; Dupont, Céline; Drunat, Séverine; Rachid, Myriam; Atzori, Paola; Delorme, Richard; Jeyarajah, Sabatini; Isidor, Bertrand; Pichon, Olivier; Moradkhani, Kamran; Verloes, Alain; Tabet, Anne-Claude.
Afiliação
  • Lévy J; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Cogan G; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Maruani A; Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France.
  • Maillard A; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Dupont C; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Drunat S; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Rachid M; INSERM U1141, Robert-Debré University Hospital, Paris, France.
  • Atzori P; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Delorme R; Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France.
  • Jeyarajah S; Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France.
  • Isidor B; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Pichon O; Service de Génétique Médicale, CHU Nantes, Nantes, France.
  • Moradkhani K; Service de Génétique Médicale, CHU Nantes, Nantes, France.
  • Verloes A; Service de Génétique Médicale, CHU Nantes, Nantes, France.
  • Tabet AC; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
Clin Genet ; 101(3): 364-370, 2022 03.
Article em En | MEDLINE | ID: mdl-34904221
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Transtorno do Espectro Autista / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Transtorno do Espectro Autista / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article