AML with translocation t(8;16)(p11;p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features
- Author
- HAFERLACH, T1 ; KOHLMANN, A1 ; HAFERLACH, C1 ; KLEIN, H.-U2 ; RUCKERT, C2 ; DUGAS, M2 ; WILLIAMS, P. M3 ; KERN, W1 ; SCHNITTGER, S1 ; BACHER, U4 ; LÖFFLER, H
[1] MLL Munich Leukemia Laboratory, Munich, Germany
[2] Department of Medical Informatics and Biomathematics, University of Münster, Münster, Germany
[3] Department of Genomics and Oncology, Roche Molecular Systems Inc, Pleasanton, CA, United States
[4] Department of Stem Cell Transplantation, University Cancer Center Hamburg, Hamburg, Germany - Source
Leukemia. 2009, Vol 23, Num 5, pp 934-943, 10 p ; ref : 55 ref
- CODEN
- LEUKED
- ISSN
- 0887-6924
- Scientific domain
- Medical oncology; Hematology
- Publisher
- Nature Publishing Group, Avenel, NJ
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- MYST3 acute leukemia gene expression microarray t(8;16)(p11;p13)
- Keyword (fr)
- Chromosome C8 anormal Cytogénétique Expression génique Hématologie Leucémie aiguë myéloblastique Leucémie aiguë Pronostic Translocation chromosomique Gène MYST3 Aberration chromosomique Cancer Chromosome anormal Hémopathie maligne
- Keyword (en)
- Abnormal chromosome C8 Cytogenetics Gene expression Hematology Acute myelogenous leukemia Acute leukemia Prognosis Chromosome translocation Chromosomal aberration Cancer Abnormal chromosome Malignant hemopathy
- Keyword (es)
- Cromosoma C8 anormal Citogenética Expresión genética Hematología Leucemia aguda mieloblástica Leucemia aguda Pronóstico Translocación cromosómica Aberración cromosómica Cáncer Cromosoma anormal Hemopatía maligna
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19B Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations
- Discipline
- Blood diseases Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 21538959
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
10.1038/leu.2008.388 
https://dx.doi.org/10.1038/leu.2008.388
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