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Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome.
Jongmans, M C J; Kuiper, R P; Carmichael, C L; Wilkins, E J; Dors, N; Carmagnac, A; Schouten-van Meeteren, A Y N; Li, X; Stankovic, M; Kamping, E; Bengtsson, H; Schoenmakers, E F P M; van Kessel, A Geurts; Hoogerbrugge, P M; Hahn, C N; Brons, P P; Scott, H S; Hoogerbrugge, N.
Leukemia ; 24(1): 242-6, 2010 Jan.
Article in En | MEDLINE | ID: mdl-19946261
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Platelet Disorders / Leukemia, Myeloid, Acute / Core Binding Factor Alpha 2 Subunit / Mutation Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Leukemia Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2010 Document type: Article Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Platelet Disorders / Leukemia, Myeloid, Acute / Core Binding Factor Alpha 2 Subunit / Mutation Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Leukemia Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2010 Document type: Article Country of publication: