Test Menu Category: Fluorescence in-situ Hybridization

Background

FISH, a molecular cytogenetic technique, enables the analysis of disease specific abnormalities. It is offered for the detection of cryptic rearrangements, microdeletion syndromes, aneuploidy, and marker chromosome identification.

This branch of cytogenetic analysis is more specific than standard karyotype analysis, enabling analysis of disease-specific abnormalities. Using results from previous testing, specific gene locations can be selected for investigation. FISH is offered for the detection of translocations, microdeletion syndromes, aneuploidy and marker chromosome identification.


Fluorescence in-situ Hybridization Tests

Myelodsyplasia Panel (MDS) by FISH

Myeloproliferative Neoplasms Panel (MPD) by FISH

Oligodendroglioma, 1p-, 19q- by FISH

PDGFRβ Gene Rearrangement by FISH

Phelan-McDermid Syndrome, deletion 22q13 by FISH*

Plasma Cell Neoplasms Panel by FISH

PML/RARA t(15,17) by FISH

Prader-Willi Syndrome deletion 15q11 by FISH*

ROS1 6q22.1 rearrangement by FISH

Smith-Magenis Syndrome deletion 17p11.2 by FISH*

SRY/CEP X deletion Yp11.3 by FISH*

Steroid Sulfatase Deficiency deletion Xp22, x-linked ichthyosis by FISH*

TEL(ETV6)/AML1(RUNX1) t(12;21) by FISH

TP53 17p13 deletion by FISH

Trisomy 5, 9,15 by FISH

Trisomy 8 by FISH

Williams Syndrome deletion 7q11.2 by FISH*

Wolf-Hirschhorn Syndrome deletion 4p16.3 by FISH*

X/Y Sex-Mismatch Transplant SRY/CEP X deletion Yp11.3 by FISH*

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