TY  - GEN
AU  - Quentin,Samuel
AU  - Cuccuini,Wendy
AU  - Ceccaldi,Raphael
AU  - Nibourel,Olivier
AU  - Pondarre,Corinne
AU  - Pagès,Marie-Pierre
AU  - Vasquez,Nadia
AU  - Dubois d'Enghien,Catherine
AU  - Larghero,Jérôme
AU  - Peffault de Latour,Régis
AU  - Rocha,Vanderson
AU  - Dalle,Jean-Hugues
AU  - Schneider,Pascale
AU  - Michallet,Mauricette
AU  - Michel,Gérard
AU  - Baruchel,André
AU  - Sigaux,François
AU  - Gluckman,Eliane
AU  - Leblanc,Thierry
AU  - Stoppa-Lyonnet,Dominique
AU  - Preudhomme,Claude
AU  - Socié,Gérard
AU  - Soulier,Jean
TI  - Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions
SN  - 1528-0020
PY  - 2011///0621
KW  - Adolescent
KW  - Adult
KW  - Bone Marrow
KW  - physiology
KW  - Child
KW  - Child, Preschool
KW  - Core Binding Factor Alpha 2 Subunit
KW  - genetics
KW  - Fanconi Anemia
KW  - complications
KW  - Female
KW  - Gene Dosage
KW  - Gene Expression Profiling
KW  - Gene Expression Regulation, Leukemic
KW  - Genes, Tumor Suppressor
KW  - Genomic Instability
KW  - Homozygote
KW  - Humans
KW  - Leukemia, Myeloid, Acute
KW  - etiology
KW  - Male
KW  - Middle Aged
KW  - Myelodysplastic Syndromes
KW  - Nucleophosmin
KW  - Polymorphism, Single Nucleotide
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1182/blood-2010-09-308726
ER  -