Presence of clone-specific markers at birth in children with acute lymphoblastic leukaemia
- Author
- HJALGRIM, L. L1 ; MADSEN, H. O2 ; SCHMIEGELOW, K7 ; HJALGRIM, H1 ; MELBYE, M1 ; JØRGENSEN, P3 ; CHRISTIANSEN, M4 ; ANDERSEN, M. T3 ; PALLISGAARD, N5 ; HOKLAND, P5 ; CLAUSEN, N6 ; RYDER, L. P2
[1] Department of Epidemiology Research, Danish Epidemiology Science Centre, Statens Serum Institut, Artilienvej 5, 2300 Copenhagen, Denmark
[2] Tissue Typing Laboratory, Department of Clinical Immunology, National University Hospital, Tagensvej 20, 2200 Copenhagen, Denmark
[3] Department of Molecular and Structural Biology, University of Aarhus, CF Møllers Allé 130, 8000 Aarhus, Denmark
[4] Department of Clinical Biochemistry, Statens Serum Institut, Artillerivej 5, 2300 Copenhagen, Denmark
[5] Department of Haematology and Medicine, Aarhus University Hospital, Tage Hansens Gade 2, 8000 Aarhus, Denmark
[6] Department of Paediatrics University Hospital of Aarhus at Skejby, Brendstrupgårdsvej 100, 8200 Aarhus, Denmark
[7] Paediatric Clinic II, Juliane Mane Centre, National University Hospital, Blegdamsvej 9, 2100 Copenhagen, Denmark - Source
British journal of cancer. 2002, Vol 87, Num 9, pp 994-999, 6 p ; ref : 22 ref
- CODEN
- BJCAAI
- ISSN
- 0007-0920
- Scientific domain
- Medical oncology
- Publisher
- Nature Publishing Group, Basingstoke
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- TEL-AML I fusion gene leukaemia prenatal origin tumour burden
- Keyword (fr)
- Aigu Cellule CFU-BL Chromosome C12 anormal Chromosome G21 anormal Clone Cytogénétique Enfant Gène hybride Leucémie lymphoblastique Origine foetale Translocation chromosomique Gène AML1 Gène TEL Aberration chromosomique Chromosome anormal Génétique Homme Hémopathie maligne Lymphoprolifératif syndrome
- Keyword (en)
- Acute CFU-BL-Cell Abnormal chromosome C12 Abnormal chromosome G21 Clone Cytogenetics Child Hybrid gene Acute lymphocytic leukemia Fetal origin Chromosome translocation Chromosomal aberration Abnormal chromosome Genetics Human Malignant hemopathy Lymphoproliferative syndrome
- Keyword (es)
- Agudo Célula CFU-BL Cromosoma C12 anormal Cromosoma G21 anormal Clona Citogenética Niño Gen híbrido Leucemia linfoblástica Origen fetal Translocación cromosómica Aberración cromosómica Cromosoma anormal Genética Hombre Hemopatía maligna Linfoproliferativo síndrome
- 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
- 14009345
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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