Your browser doesn't support javascript.
loading
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Tabet, Anne-Claude; Rolland, Thomas; Ducloy, Marie; Lévy, Jonathan; Buratti, Julien; Mathieu, Alexandre; Haye, Damien; Perrin, Laurence; Dupont, Céline; Passemard, Sandrine; Capri, Yline; Verloes, Alain; Drunat, Séverine; Keren, Boris; Mignot, Cyril; Marey, Isabelle; Jacquette, Aurélia; Whalen, Sandra; Pipiras, Eva; Benzacken, Brigitte; Chantot-Bastaraud, Sandra; Afenjar, Alexandra; Héron, Delphine; Le Caignec, Cédric; Beneteau, Claire; Pichon, Olivier; Isidor, Bertrand; David, Albert; El Khattabi, Laila; Kemeny, Stephan; Gouas, Laetitia; Vago, Philippe; Mosca-Boidron, Anne-Laure; Faivre, Laurence; Missirian, Chantal; Philip, Nicole; Sanlaville, Damien; Edery, Patrick; Satre, Véronique; Coutton, Charles; Devillard, Françoise; Dieterich, Klaus; Vuillaume, Marie-Laure; Rooryck, Caroline; Lacombe, Didier; Pinson, Lucile; Gatinois, Vincent; Puechberty, Jacques; Chiesa, Jean; Lespinasse, James.
Afiliação
  • Tabet AC; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Rolland T; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
  • Ducloy M; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
  • Lévy J; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.
  • Buratti J; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
  • Mathieu A; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
  • Haye D; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.
  • Perrin L; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
  • Dupont C; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
  • Passemard S; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.
  • Capri Y; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Verloes A; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
  • Drunat S; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
  • Keren B; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.
  • Mignot C; 2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
  • Marey I; 3CNRS UMR 3571 Genes, Synapses and Cognition, Institut Pasteur, Paris, France.
  • Jacquette A; 4Sorbonne Paris Cité, Human Genetics and Cognitive Functions, Université Paris Diderot, Paris, France.
  • Whalen S; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Pipiras E; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Benzacken B; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Chantot-Bastaraud S; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Afenjar A; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Héron D; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Le Caignec C; 1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
  • Beneteau C; 5Cytogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
  • Pichon O; 6Neurogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
  • Isidor B; 7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
  • David A; 7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
  • El Khattabi L; 7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
  • Kemeny S; 8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France.
  • Gouas L; 8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France.
  • Vago P; 9Cytogenetics Unit, Trousseau Hospital, APHP, Paris, France.
  • Mosca-Boidron AL; 10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France.
  • Faivre L; 10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France.
  • Missirian C; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
  • Philip N; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
  • Sanlaville D; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
  • Edery P; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
  • Satre V; 11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
  • Coutton C; 12Cytogenetics Unit, Cochin Hospital, APHP, Paris, France.
  • Devillard F; 13Genetics Unit, CHU Estaing, Clermont-Ferrand, France.
  • Dieterich K; 13Genetics Unit, CHU Estaing, Clermont-Ferrand, France.
  • Vuillaume ML; 13Genetics Unit, CHU Estaing, Clermont-Ferrand, France.
  • Rooryck C; Cytogenetics Unit, Dijon Hospital, Dijon, France.
  • Lacombe D; Clinical Genetics Unit, Dijon Hospital, Dijon, France.
  • Pinson L; 16Genetics Unit, La Timone Hospital, Marseille, France.
  • Gatinois V; 16Genetics Unit, La Timone Hospital, Marseille, France.
  • Puechberty J; Cytogenetics Unit, Lyon Civil Hospital, Lyon, France.
  • Chiesa J; Clinical Genetics Unit, Lyon Civil Hospital, Lyon, France.
  • Lespinasse J; 19Cytogenetics Unit, Grenoble Hospital, Grenoble, France.
NPJ Genom Med ; 4: 16, 2019.
Article em En | MEDLINE | ID: mdl-31285849
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: NPJ Genom Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: NPJ Genom Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França