RUNX1 gene mutation in primary myelodysplastic syndrome -the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome
- Author
- CHEN, Chien-Yuan1 ; LIN, Liang-In2 3 ; TANG, Jih-Luh1 ; KO, Bo-Sheng1 ; TSAY, Woei1 ; CHOU, Wen-Chien1 2 ; MING YAO1 ; WU, Shang-Ju1 ; TSENG, Mei-Hsuan1 ; TIEN, Hwei-Fang1
[1] Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan, Province of China
[2] Laboratory Medicine National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan, Province of China
[3] Department of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, Taiwan, Province of China - Source
British journal of haematology. 2007, Vol 139, Num 3, pp 405-414, 10 p ; ref : 1 p.1/4
- CODEN
- BJHEAL
- ISSN
- 0007-1048
- Scientific domain
- Medical oncology; Hematology
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- RUNX1 mutation myelodysplastic syndrome sequential follow-up
- Keyword (fr)
- Acquis Diagnostic Génétique Hématologie Mutation Myélodysplasique syndrome Primaire Pronostic Stade précoce Séquentiel Gène AML1 Hémopathie maligne
- Keyword (en)
- Acquired Diagnosis Genetics Hematology Mutation Myelodysplastic syndrome Primary Prognosis Early stage Sequential Malignant hemopathy
- Keyword (es)
- Adquirido Diagnóstico Genética Hematología Mutación Mielodisplastico síndrome Primario Pronóstico Estadio precoz Secuencial Hemopatía maligna
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19B Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 19156124
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1111/j.1365-2141.2007.06811.x 
https://dx.doi.org/10.1111/j.1365-2141.2007.06811.x
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