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FGFR1/CSP8 FISH Probe

The FGFR1/CSP8 FISH Probe is intended for use to qualitatively detect the FGFR1 gene amplification/deletion via fluorescence in situ hybridization (FISH) methodology in sections of formalin-fixed paraffin-embedded (FFPE) tissue or peripheral blood smears specimens

Cat#

LCFS-138
Chromosomal Localization

CSP8
Clinical Relevance

This gene is linked to Pfeiffer, Jackson-Weiss, Antley-Bixler syndromes, osteoglophonic dysplasia, Kallmann syndrome type 2, and chromosomal changes causing stem cell disorders and lymphoma.
Probe Type

Amplification/Deletion
Sizes

5; 10; 20 tests
Synonyms

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