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Updated: Aug 19, 2026

Simple Method for Fluorescence DNA In Situ Hybridization to Squashed Chromosomes
Published on: January 6, 2015
Gene identification by chromosomal in-situ hybridization, microdissection and polymerase chain reaction amplification
1Liver Unit, National Institute for Health, Bethesda, Maryland 20892, USA. RichardS@BDG10.NIDDK.NIH.gov
Abstract:
This paper describes a theoretical method by which candidate genes for inherited diseases can be identified by polymerase chain reaction amplification and subsequent cloning of organ-specific complementary deoxyribonucleic acid libraries hybridized in situ to, and subsequently dissected from, the cognate chromosome. A specific application of this technique to isolate genes related to genetic haemochromatosis is outlined.
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