Diagnosis of cryptic chromosomal syndromes by fluorescence in situ hybridization (FISH).

Diagnosis of cryptic chromosomal syndromes by fluorescence in situ hybridization (FISH).
Curr Protoc Hum Genet. 2010 Oct;Chapter 8:Unit 8.10.1-20
Authors: Kashork CD, Theisen A, Shaffer LG
Abstract
This unit describes the various methods by which cytogeneticists detect chromosome abnormalities. The unit offers guidance for detecting such abnormalities with fluorescence in situ hybridization (FISH), as well as the benefits, limitations, and other applications of FISH.
PMID: 20891031 [PubMed - indexed for MEDLINE]

Source: Current Protocols in Human Genetics - November 25, 2014 Category: Genetics & Stem Cells Tags: Curr Protoc Hum Genet Source Type: research