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Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group.
Aronson, Melyssa; Colas, Chrystelle; Shuen, Andrew; Hampel, Heather; Foulkes, William D; Baris Feldman, Hagit; Goldberg, Yael; Muleris, Martine; Wolfe Schneider, Kami; McGee, Rose B; Jasperson, Kory; Rangaswami, Arun; Brugieres, Laurence; Tabori, Uri.
Afiliación
  • Aronson M; Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, Ontario, Canada Melyssa.Aronson@sinaihealth.ca.
  • Colas C; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Shuen A; Département de génétique, Institut Curie, Université Paris Sciences Lettres, Paris, France.
  • Hampel H; Sickkids, Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Foulkes WD; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
  • Baris Feldman H; Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Goldberg Y; Program in Cancer Genetics, Departments of Human Genetics and Oncology, McGill University, Montreal, Quebec, Canada.
  • Muleris M; The Genetics Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Wolfe Schneider K; Tel Aviv University Sackler Faculty of Medicine, Tel Aviv, Israel.
  • McGee RB; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Jasperson K; The Raphael Recanati Genetic Institute, Rabin Medical Center - Beilinson Hospital, Petah Tikva, Israel.
  • Rangaswami A; Inserm, Centre de Recherche Saint-Antoine, CRSA, Sorbonne Université, Paris, France.
  • Brugieres L; Section of Hematology, Oncology and Bone Marrow Transplantation, Children's Hospital Colorado, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, USA.
  • Tabori U; Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
J Med Genet ; 59(4): 318-327, 2022 04.
Article en En | MEDLINE | ID: mdl-33622763
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Neoplasias Encefálicas / Neoplasias Colorrectales Tipo de estudio: Diagnostic_studies / Guideline / Systematic_reviews Límite: Humans Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Neoplásicos Hereditarios / Neoplasias Encefálicas / Neoplasias Colorrectales Tipo de estudio: Diagnostic_studies / Guideline / Systematic_reviews Límite: Humans Idioma: En Revista: J Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido