Skip to search formSkip to main contentSkip to account menu

t(2;13)

A cytogenetic abnormality that involves a translocation between chromosomes 2 and 13.
National Institutes of Health

Related topics

Related topics

2 relations
Chromosomes, Human, Pair 13Chromosomes, Human, Pair 2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Downregulation of miR-15a and miR-16-1 at 13q14 in Chronic Lymphocytic Leukemia.
Featured Article: Calin GA, Dumitru CD, Shimizu M, Bichi R, Zupo S, Noch E, et al. Frequent deletions and down-regulation of… 
2009
2009
Translocation (2;13) and other chromosome abnormalities in intraosseous schwannoma of the mandible.
2000
2000
Structural analysis of PAX7 rearrangements in alveolar rhabdomyosarcoma.
1998
1998
Solid alveolar rhabdomyosarcoma of the thorax in a child
This case illustrates the difficulties and pitfalls of diagnosis of alveolar rhabdomyosarcoma in its solid variant and in an… 
1997
1997
Relevance of cytogenetic and fluorescent in situ hybridization analyses in the clinical assessment of soft tissue sarcoma.
Review
1997
Review
1997
Chromosomal translocations involving paired box transcription factors in human cancer.
1997
1997
Regulated expression of the diphtheria toxin A chain by a tumor-specific chimeric transcription factor results in selective toxicity for alveolar rhabdomyosarcoma cells.
Alveolar rhabdomyosarcoma (ARMS) cells often harbor one of two unique chromosomal translocations, either t(2;13)(q35;q14) or t(1… 
1990
1990
A NOVEL VARIANT TRANSLOCATION t(2;13) (p23;q34) IN Ki‐1 LARGE CELL ANAPLASTIC LYMPHOMA
Recently a large cell lymphoma, strongly reacting with Ki-1 (CD 30) monoclonal antibody (MoAb), has been described (Stein et al… 
1989
1989
Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma.
A specific chromosomal translocation, t(2;13)(q35;q14), is present in tumor cells from about one-half of children with alveolar… 
1977
1977
[Partial trisomy 13 due to maternal translocation t(2;13)].
The authors report an observation of partial trisomy 13p13 leads to qter and suggest a clinical map of chromosome 13. Increase of… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)