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Updated: Feb 9, 2026

Simple Method for Fluorescence DNA In Situ Hybridization to Squashed Chromosomes
Published on: January 6, 2015
Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation
R Wallerstein1, L Gibas, C E Anderson
1Division of Medical Geńetics, Jefferson Medical College of Thomas Jefferson University, Philadelphia, PA 19107-5563, USA.
Abstract:
We report the use of fluorescent in situ hybridisation (FISH) to clarify a complex chromosomal rearrangement (CCR) carried by a woman presenting with recurrent miscarriages. CCRs are rare cytogenetic rearrangements involving three or more chromosomes, which can be difficult to interpret using routine cytogenetic studies with GTG banding. FISH was used to establish a correct interpretation of the maternal karyotype before amniocentesis in a present pregnancy.
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