Mrózek, K <br/><br/>
Spectral karyotyping reveals 17;22 fusions in a cytogenetically atypical dermatofibrosarcoma protuberans with a large marker chromosome as a sole abnormality.  [electronic resource] 

 -  Genes, chromosomes & cancer  Jun 2001 
 - 182-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1045-2257 
<br/><br/><label>Standard No.: </label>10.1002/gcc.1131  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Painting<br/>Chromosomes, Human, Pair 17--genetics<br/>Chromosomes, Human, Pair 22--genetics<br/>Chromosomes, Human, Pair 8--genetics<br/>Dermatofibrosarcoma--genetics<br/>Female<br/>Genetic Markers--genetics<br/>Humans<br/>Karyotyping--methods<br/>Neoplasm Recurrence, Local<br/>Ring Chromosomes<br/>Skin Neoplasms--genetics<br/>Translocation, Genetic--genetics