Document Detail

Is t(6;14) a non-random translocation in childhood acute mixed lineage leukemia?
MedLine Citation:
PMID:  8780743     Owner:  NLM     Status:  MEDLINE    
We report a case of childhood acute mixed lineage leukemia (AMLL) with a translocation t(6;14)(q25;q32) as the main clonal abnormality. A comparison of this case with another one with similar cytogenetics and clinical findings may suggest that t(6;14)(q25;q32) is a non-random occurrence in childhood AMLL.
J R Batanian; C H Dunphy; G Gale; N Havlioglu
Related Documents :
8562943 - Leukemia-associated changes identified by quantitative flow cytometry. iv. cd34 overexp...
24419983 - Teaching neuroimages: facial diplegia due to neuroborreliosis.
17319593 - Nonconvulsive status epilepticus causing prolonged stupor after intraventricular hemorr...
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Cancer genetics and cytogenetics     Volume:  90     ISSN:  0165-4608     ISO Abbreviation:  Cancer Genet. Cytogenet.     Publication Date:  1996 Aug 
Date Detail:
Created Date:  1996-10-16     Completed Date:  1996-10-16     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  7909240     Medline TA:  Cancer Genet Cytogenet     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  29-32     Citation Subset:  IM    
Pediatrics Department, Saint Louis University Hospital, Missouri, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Acute Disease
Bone Marrow / pathology
Chromosomes, Human, Pair 14 / ultrastructure*
Chromosomes, Human, Pair 6 / ultrastructure*
In Situ Hybridization, Fluorescence
Leukemia, Biphenotypic, Acute / genetics*,  pathology
Translocation, Genetic*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  A case of acute myelofibrosis with complex karyotypic changes: a type of myelodysplastic syndrome.
Next Document:  Complex cytogenetic and immunophenotypic aberrations in a patient with Sezary syndrome.