CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)

Blood

Volumn 119, Issue 11, 2012, Pages 2612-2614

  Shiba, Norio ^a,b   Hasegawa, Daisuke ^c   Park, Myoung Ja ^a   Murata, Chisato ^a   Sato Otsubo, Aiko ^d   Ogawa, Chitose ^c   Manabe, Atsushi ^c   Arakawa, Hirokazu ^b   Ogawa, Seishi ^d   Hayashi, Yasuhide ^a  

^a Gumna Children S Medical Center   (Japan)

^b GUNMA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c ST LUKE'S INTERNATIONAL HOSPITAL   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR RUNX1;

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; ARTICLE; CASE REPORT; CBL GENE; CHILD; CHROMOSOME 11Q; CHRONIC MYELOMONOCYTIC LEUKEMIA; FAMILIAL DISEASE; FEMALE; GENE; GENE MUTATION; HUMAN; MALIGNANT TRANSFORMATION; MUTATIONAL ANALYSIS; PATHOGENESIS; PEDIGREE; PRIORITY JOURNAL; THROMBOCYTE DISORDER; UNIPARENTAL DISOMY;

EID: 84858684845     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2011-02-333435     Document Type: Article

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