首页> European journal of medical genetics> Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis.

Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis.

导出 LinkOut

翻译打印收藏纠错

第一作者： François,Lecoquierre

第一单位： 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.

作者： François,Lecoquierre ^[1] ; Kévin,Cassinari ^[2] ; Pascal,Chambon ^[2] ; Gaël,Nicolas ^[2] ; Sarah,Malsa ^[3] ; Régine,Marlin ^[3] ; Yvon,Assouline ^[4] ; Jean-François,Fléjou ^[5] ; Thierry,Frebourg ^[2] ; Claude,Houdayer ^[2] ; Odile,Bera ^[3] ; Stéphanie,Baert-Desurmont ^[2]

作者单位： 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. ^[1] 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. ^[2] Department of Cancer Genetics, Martinique University Hospital, Fort-de-France, Martinique, France. ^[3] Departement of Gastro-Enterology, Clinique Saint Paul, Fort-de-France, Martinique, France. ^[4] Pathology Department, AP-HP, Hôpital Saint-Antoine, Faculté de Médecine Sorbonne Université, Paris, France. ^[5]