eagle-i Oregon Health & Science UniversityOregon Health & Science University
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Williams Syndrome detection using FISH protocol

eagle-i ID


Resource Type

  1. Protocol


  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
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The eagle-i Consortium is supported by NIH Grant #5U24RR029825-02 / Copyright 2016