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Translocation t(12;19)(q13;q13.3): a new recurrent abnormality in acute nonlymphocytic leukemia with atypical erythropoiesis

Author
PAIETTA, E1 ; PAPENHAUSEN, P; RASIM GUCALP; WIERNIK, P. H
[1] Montefiore medical cent., dep. oncology, Bronx NY 10467, United States
Source

Cancer genetics and cytogenetics. 1988, Vol 34, Num 1, pp 19-23 ; ref : 11 ref

CODEN
CGCYDF
ISSN
0165-4608
Scientific domain
Medical oncology; Genetics
Publisher
Elsevier Science, New York, NY
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Aigu Chromosome C12 anormal Chromosome F19 anormal Cytogénétique Erythropoïèse Homme Hémopathie Leucémie non lymphocytaire Moelle osseuse Récidive Translocation chromosomique T(12;19) Aberration chromosomique Chromosome anormal
Keyword (en)
Acute Abnormal C12 chromosome Abnormal «F19» chromosome Cytogenetics Erythropoiesis Human Hemopathy Nonlymphocytic leukemia Bone marrow Recurrence Chromosome translocation Abnormal chromosome Chromosomal aberration
Keyword (es)
Agudo Cromosoma C12 anormal Cromosoma F19 anormal Citogenética Eritropoyesis Hombre Hemopatía Leucemia no linfocitaria Médula ósea Recidiva Translocación cromosómica Aberración cromosómica Cromosoma anormal
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
7788290

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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