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Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.
Sarasin, Alain; Quentin, Samuel; Droin, Nathalie; Sahbatou, Mourad; Saada, Véronique; Auger, Nathalie; Boursin, Yannick; Dessen, Philippe; Raimbault, Anna; Asnafi, Vahid; Schmutz, Jean-Luc; Taïeb, Alain; Menck, Carlos F M; Rosselli, Filippo; La Rochelle, Laurianne Drieu; Robert, Caroline; Sicre de Fontbrune, Flore; Sébert, Marie; Leblanc, Thierry; Kannouche, Patricia; De Botton, Stéphane; Solary, Eric; Soulier, Jean.
Afiliação
  • Sarasin A; Laboratory of Genetic Instability and Oncogenesis, Unité Mixte de Recherche 8200 Centre National de la Recherche Scientifique, University Paris-Sud and Gustave Roussy, Villejuif, France.
  • Quentin S; Institut National de la Santé et de la Recherche Médicale/CNRS U944/7212 and University Paris Diderot, University of Paris, France.
  • Droin N; Hematology Laboratory, Saint-Louis Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Sahbatou M; Centre de référence Maladies Rares des Aplasies médullaires, Hôpital Saint-Louis et Robert Debré, Paris, France.
  • Saada V; INSERM U1170, Gustave Roussy, Université Paris-Sud, Villejuif, France.
  • Auger N; Gustave Roussy, Université Paris-Saclay, Département d'hématologie, Villejuif, France.
  • Boursin Y; Fondation Jean Dausset, Centre d'Etude du Polymorphisme Humain, Paris, France.
  • Dessen P; Département de biologie et pathologie médicales, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Raimbault A; Département de biologie et pathologie médicales, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Asnafi V; Bioinformatics Core Facility, Gustave Roussy, Villejuif, France.
  • Schmutz JL; Bioinformatics Core Facility, Gustave Roussy, Villejuif, France.
  • Taïeb A; Institut National de la Santé et de la Recherche Médicale/CNRS U944/7212 and University Paris Diderot, University of Paris, France.
  • Menck CFM; Hematology Laboratory, Saint-Louis Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Rosselli F; Centre de référence Maladies Rares des Aplasies médullaires, Hôpital Saint-Louis et Robert Debré, Paris, France.
  • La Rochelle LD; Institut Necker-Enfants Malades, INSERM U1151, Paris, France.
  • Robert C; Department of Dermatology, Nancy University Hospital, Vandoeuvre-Lès-Nancy, France.
  • Sicre de Fontbrune F; Department of Dermatology, Bordeaux University Hospitals, and INSERM U1035, University of Bordeaux, Bordeaux, France.
  • Sébert M; Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil.
  • Leblanc T; Laboratory of Genetic Instability and Oncogenesis, Unité Mixte de Recherche 8200 Centre National de la Recherche Scientifique, University Paris-Sud and Gustave Roussy, Villejuif, France.
  • Kannouche P; Service d'Hématologie, CHU de Tours, Tours, France.
  • De Botton S; Department of Dermatology, Gustave Roussy, Villejuif, France.
  • Solary E; Centre de référence Maladies Rares des Aplasies médullaires, Hôpital Saint-Louis et Robert Debré, Paris, France.
  • Soulier J; Hematology/Transplantation and.
Blood ; 133(25): 2718-2724, 2019 06 20.
Article em En | MEDLINE | ID: mdl-30914417
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Xeroderma Pigmentoso / Síndromes Mielodisplásicas / Leucemia / Predisposição Genética para Doença Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Xeroderma Pigmentoso / Síndromes Mielodisplásicas / Leucemia / Predisposição Genética para Doença Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article