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Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia.
Cavé, Hélène; Caye, Aurélie; Ghedira, Nehla; Capri, Yline; Pouvreau, Nathalie; Fillot, Natacha; Trimouille, Aurélien; Vignal, Cédric; Fenneteau, Odile; Alembik, Yves; Alessandri, Jean-Luc; Blanchet, Patricia; Boute, Odile; Bouvagnet, Patrice; David, Albert; Dieux Coeslier, Anne; Doray, Bérénice; Dulac, Olivier; Drouin-Garraud, Valérie; Gérard, Marion; Héron, Delphine; Isidor, Bertrand; Lacombe, Didier; Lyonnet, Stanislas; Perrin, Laurence; Rio, Marlène; Roume, Joëlle; Sauvion, Sylvie; Toutain, Annick; Vincent-Delorme, Catherine; Willems, Marjorie; Baumann, Clarisse; Verloes, Alain.
Afiliação
  • Cavé H; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Caye A; INSERM UMR S1131, Institut Universitaire d'Hématologie, Denis Diderot Medical School, Sorbonne-Paris-Cité University, Paris, France.
  • Ghedira N; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Capri Y; INSERM UMR S1131, Institut Universitaire d'Hématologie, Denis Diderot Medical School, Sorbonne-Paris-Cité University, Paris, France.
  • Pouvreau N; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Fillot N; INSERM UMR S1131, Institut Universitaire d'Hématologie, Denis Diderot Medical School, Sorbonne-Paris-Cité University, Paris, France.
  • Trimouille A; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Vignal C; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Fenneteau O; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Alembik Y; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Alessandri JL; INSERM UMR S1131, Institut Universitaire d'Hématologie, Denis Diderot Medical School, Sorbonne-Paris-Cité University, Paris, France.
  • Blanchet P; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Boute O; Hematology Laboratory, AP-HP - Robert Debré University Hospital, Paris, France.
  • Bouvagnet P; Department of Genetics, University Hospital, Strasbourg, France.
  • David A; Department of Genetics, University Hospital, Saint Denis de la Réunion, France.
  • Dieux Coeslier A; Department of Genetics, University Hospital, Montpellier, France.
  • Doray B; Department of Genetics, Jeanne de Flandre University Hospital, Lille, France.
  • Dulac O; Medico-surgical Department of Child and Adult Cardiology, Louis Pradel University Hospital, Lyon University, Bron, France.
  • Drouin-Garraud V; Department of Genetics, University Hospital, Nantes, France.
  • Gérard M; Department of Genetics, Jeanne de Flandre University Hospital, Lille, France.
  • Héron D; Department of Genetics, University Hospital, Strasbourg, France.
  • Isidor B; Department of Child Neurology, AP-HP-Necker-Enfants Malades Hospital, Paris, France.
  • Lacombe D; Department of Genetics, University Hospital, Rouen, France.
  • Lyonnet S; Department of Genetics, University Hospital, Caen, France.
  • Perrin L; Department of Genetics, AP-HP - La Pitié-Salpétrière Hospital, Paris, France.
  • Rio M; Department of Genetics, University Hospital, Nantes, France.
  • Roume J; Department of Genetics, University Hospital, Bordeaux, France.
  • Sauvion S; Department of Genetics, AP-HP - Necker-Enfants Malades Hospital, Paris, France.
  • Toutain A; Department of Genetics, Assistance Publique - Hôpitaux de Paris (AP-HP) - Robert Debré University Hospital, Paris, France.
  • Vincent-Delorme C; Department of Genetics, AP-HP - Necker-Enfants Malades Hospital, Paris, France.
  • Willems M; Department of Genetics, Intercommunal Hospital, Poissy-St Germain en Laye, France.
  • Baumann C; Department of Pediatrics, AP-HP - Jean Verdier Hospital, Bondy, France.
  • Verloes A; Department of Genetics, University Hospital, Tours, France.
Eur J Hum Genet ; 24(8): 1124-31, 2016 08.
Article em En | MEDLINE | ID: mdl-26757980
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas ras / Leucemia-Linfoma Linfoblástico de Células Precursoras / Leucemia Mielomonocítica Juvenil / Mutação / Síndrome de Noonan Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas ras / Leucemia-Linfoma Linfoblástico de Células Precursoras / Leucemia Mielomonocítica Juvenil / Mutação / Síndrome de Noonan Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2016 Tipo de documento: Article