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Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.
Quentin, Samuel; Cuccuini, Wendy; Ceccaldi, Raphael; Nibourel, Olivier; Pondarre, Corinne; Pagès, Marie-Pierre; Vasquez, Nadia; Dubois d'Enghien, Catherine; Larghero, Jérôme; Peffault de Latour, Régis; Rocha, Vanderson; Dalle, Jean-Hugues; Schneider, Pascale; Michallet, Mauricette; Michel, Gérard; Baruchel, André; Sigaux, François; Gluckman, Eliane; Leblanc, Thierry; Stoppa-Lyonnet, Dominique; Preudhomme, Claude; Socié, Gérard; Soulier, Jean.
Affiliation
  • Quentin S; Team Genome and Cancer, Hematology Laboratory Assistance Publique-Hopitaux de Paris, Saint-Louis Hospital, Paris, France.
Blood ; 117(15): e161-70, 2011 Apr 14.
Article in En | MEDLINE | ID: mdl-21325596
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myelodysplastic Syndromes / Leukemia, Myeloid, Acute / Genomic Instability / Core Binding Factor Alpha 2 Subunit / Fanconi Anemia Type of study: Etiology_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2011 Type: Article Affiliation country: France
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myelodysplastic Syndromes / Leukemia, Myeloid, Acute / Genomic Instability / Core Binding Factor Alpha 2 Subunit / Fanconi Anemia Type of study: Etiology_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2011 Type: Article Affiliation country: France