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Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.

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作者单位: Department of Genetics, Normandy Center for Genomic and Personalized Medicine, Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Rouen, France. [1] Comprehensive Cancer Center François Baclesse, Laboratory of Cancer Biology and Genetics, Caen, France. [2] Department of Biochemistry and Molecular Biology, Lille University Hospital Center, UMR 1277 Inserm-9020 CNRS, Lille University, Lille, France. [3] Medical genetics Department, Henri Mondor Hospital, Créteil, France. [4] Cancer Genetics Unit, Institut Bergonie, Bordeaux, France. [5] Department of Genetics, Hôpitaux Universitaires Pitié Salpêtrière-Charles Foix, Paris, France. [6] Gastroenterology Unit, Cochin University Hospital, Paris Descartes University, Paris, France. [7] Institut Curie, Department of Genetics and Paris Sciences, Lettres Research University, Paris, France. [8] Department of Tumor Biology and Pathology, Georges-François Leclerc Center, Dijon, France. [9] Department of Oncogenetics, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France. [10] Department of Genetics, Le Havre General Hospital, Normandy Centre for Genomic and Personalized Medicine, Le Havre, France. [11] Genetic Pathology Biology Department, Lille University Hospital Center, Jeanne de Flandre Hospital, Lille, France. [12] Department of Genetics, Rennes University Hospital Center, Rennes, France. [13] Genetics Department, Hospices Civils de LYON (HCL), University Hospital, East Pathology Center, Bron, France. [14] Oncogenetic Laboratory, Cancer University Institute Toulouse Oncopole, Toulouse, France. [15] Department of Pathology and Oncobiology, Montpellier University Hospital, Montpellier, France. [16] Centre Jean Perrin, Oncogenetics and Clermont Auvergne University, INSERM U1240, Clermont-Ferrand, France. [17]
DOI 10.1111/cge.13925
PMID 33454955
发布时间 2022-01-31
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