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Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis.
Lecoquierre, François; Cassinari, Kévin; Chambon, Pascal; Nicolas, Gaël; Malsa, Sarah; Marlin, Régine; Assouline, Yvon; Fléjou, Jean-François; Frebourg, Thierry; Houdayer, Claude; Bera, Odile; Baert-Desurmont, Stéphanie.
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  • Lecoquierre F; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France. Electronic address: francois.lecoquierre@chu-rouen.fr.
  • Cassinari K; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France.
  • Chambon P; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France.
  • Nicolas G; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France.
  • Malsa S; Department of Cancer Genetics, Martinique University Hospital, Fort-de-France, Martinique, France.
  • Marlin R; Department of Cancer Genetics, Martinique University Hospital, Fort-de-France, Martinique, France.
  • Assouline Y; Departement of Gastro-Enterology, Clinique Saint Paul, Fort-de-France, Martinique, France.
  • Fléjou JF; Pathology Department, AP-HP, Hôpital Saint-Antoine, Faculté de Médecine Sorbonne Université, Paris, France.
  • Frebourg T; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France.
  • Houdayer C; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France.
  • Bera O; Department of Cancer Genetics, Martinique University Hospital, Fort-de-France, Martinique, France.
  • Baert-Desurmont S; Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, Normandy Center for Genomic and Personalized Medicine, F76000, Rouen, France.
Eur J Med Genet ; 63(4): 103773, 2020 Apr.
Article en En | MEDLINE | ID: mdl-31561016
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Deleción Cromosómica / Mutación Puntual / Trastornos de los Cromosomas / Poliposis Intestinal / Fosfohidrolasa PTEN / Receptores de Proteínas Morfogenéticas Óseas de Tipo 1 Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Deleción Cromosómica / Mutación Puntual / Trastornos de los Cromosomas / Poliposis Intestinal / Fosfohidrolasa PTEN / Receptores de Proteínas Morfogenéticas Óseas de Tipo 1 Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article