| Literature DB >> 1652538 |
S F De Cabo1, P Ludeña, M Velázquez, C Sentis, J Fernández-Piqueras.
Abstract
Ten phenotypically normal human individuals have been analysed by in situ treatments with restriction endonucleases in order to obtain a better characterization of some cryptic variants of acrocentric chromosomes. Treatments with AluI, NdeII and Sau3AI confirm the existence of two cryptic amplified regions on the short arms of both one chromosome 15 and one chromosome 22, in one female. These amplifications seem to be of different origin involving the nucleolar organizer region of chromosome 15 and the satellite of chromosome 22.Entities:
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Year: 1991 PMID： 1652538 DOI： 10.1007/bf00126226
Source DB: PubMed Journal: Genetica ISSN： 0016-6707 Impact factor: 1.082