Skip to search formSkip to main contentSkip to account menu

t(21;22)

A cytogenetic abnormality that involves a translocation between chromosomes 21 and 22.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Review
2005
Review
2005
Ewing's sarcoma family of tumors (ESFT) affect patients between the ages of 3 and 40 years, with most cases occurring in the… 
Highly Cited
1998
Highly Cited
1998
PURPOSE Gene fusions that result from the chromosome translocations observed in Ewing's tumor (ET) provide tumor-specific markers… 
Review
1997
Review
1997
Abstract Soft tissue tumours represent a heterogeneous group of mesenchymal lesions, and their classification is the subject of… 
Review
1995
Review
1995
  • M. Ladanyi
  • Diagnostic molecular pathology : the American…
  • 1995
  • Corpus ID: 22915567
Many types of sarcomas are characterized by specific chromosomal translocations which are likely to be of etiologic significance… 
Highly Cited
1995
Highly Cited
1995
Accurate diagnosis of primitive childhood sarcomas continues to be a formidable problem because these malignancies generally… 
Highly Cited
1995
Highly Cited
1995
Cytogenetic analysis of Ewing's sarcoma, primitive neuroectodermal tumors and Askin tumors revealed characteristic translocations… 
Highly Cited
1995
Highly Cited
1995
The ETS related gene, ERG, is one of 20 or more genes belonging to the ETS family of transcription factors. Translocation of the… 
Highly Cited
1994
Highly Cited
1994
The t(11;22)(q24;q12), present in 85% of Ewing's sarcoma and related tumours, fuses the EWS gene from chromosome 22q12 and the…