Williams Syndrome detection using FISH protocol

eagle-i ID

Resource Type

Properties

1. Resource Description

   Fluorescent In-Situ Hybridization methods combine both molecular and cytogenetic techniques. They are employed to delineate subtle syndrome related chromosome defects. Williams syndrome probes are used to examine chromosome 7 for deletion of the elastin gene.

2. Uses

   Fluorescent in situ hybridization

3. Used by

   Clinical Cytogenetics Laboratory