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Trisomy 20 is a primary chromosome aberration in desmoid tumors

✍ Scribed by Fredrik Mertens; Helena Willén; Anders Rydholm; Otte Brosjö; Birgitta Carlén; Felix Mitelman; Nils Mandahl


Publisher
John Wiley and Sons
Year
1995
Tongue
French
Weight
794 KB
Volume
63
Category
Article
ISSN
0020-7136

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✦ Synopsis


Cytogenetic analysis revealed trisomy 20 in 4 desmoid tumors: in 2 cases as the sole aberration, in I together with +X, -Y and -I 3 and in I with +8 and a supernumerary marker chromosome. Our findings indicate that gain of chromosome 20 is an early event in the development of a large subset of desmoid tumors and that it is as frequent as +8, the only consistent chromosomal change previously reported in this tumor type.


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Trisomy 12 is a consistent chromosomal a
✍ Dr. Tanja Pejovic; Sverre Heim; Nils Mandahl; Bengt Elmfors; Ulla-Maria Flodérus 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 422 KB

## Abstract Clonal karyotypic abnormalities were detected in 7 of 42 cytogenetically analyzed benign ovarian tumors. An adenofibroma had –X and a mucinous cystadenoma had t(1;11)(q25;q23) as the sole abnormality. Trisomy 12 was found in the remaining five tumors. It was the only change in two fibro