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 The Cytogenetic Laboratory is currently offering FISH analysis for the following disorders. Each test in the menu includes information on indications for testing, assay methodology, specimen requirements, transport and shipping instructions, and billing codes. All specimens submitted for analysis should be accompanied by the UCSD Medical Genetics Test Requisition Form.
> Angelman Syndrome
> BCR/ABL Fusion
> CCND1/IGH
> CLL Panel
> Cri du Chat Syndrome
> DiGeorge/VCFS Syndrome
> Fetal Aneuploidy Screen
> Miller-Dieker Syndrome
> Prader-Willi Syndrome
> RARA Flanking Probes
> Smith-Magenis Syndrome
> STS/Kallman Syndrome
> Williams Syndrome (Elastin)
Please contact us to inquire about additional tests.
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