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Vysis introduces new fluorescence in situ hybridisation (FISH) probe for Williams Syndrome

This article was originally published in Clinica

Executive Summary

A dual-colour, DNA probe that relies on fluorescence in situ hybridisation (FISH) to identify the microdeletions on Chromosome 7 that are typical of Williams Syndrome was introduced last month at the 46th annual meeting of the American Society of Human Genetics.

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