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Variant translocation t(6;10)(p21;q22) in pulmonary chondroid hamartoma
Author(s) -
Minoletti Fabiola,
Sozzi Gabriella,
Calderone Carla,
Di Palma Silvana,
Pilotti Silvana,
Azzarelli Alberto,
Pierotti Marco A.
Publication year - 1996
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/(sici)1098-2264(199604)15:4<246::aid-gcc6>3.0.co;2-1
Subject(s) - chromosomal translocation , cytogenetics , fluorescence in situ hybridization , hamartoma , biology , pathology , karyotype , comparative genomic hybridization , microbiology and biotechnology , gene , genetics , chromosome , medicine
Banding cytogenetics and fluorescence in situ hybridization analysis of a pulmonary chondroid hamartoma (PCH) showed the presence of a t(6;10)(p21;q22). A cytogenetically identical translocation has previously been found in another case of PCH, suggesting that it could represent a variant form of the standard t(6;14)(p21;q24). Genes Chromosom Cancer 15:246–248 (1996). © 1996 Wiley‐Liss, Inc.