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FGFR2/CSP10 FISH Probe

The FGFR2/CSP10 FISH Probe is intended for use to qualitatively detect the FGFR2 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-140
Chromosomal Localization

CSP10
Clinical Relevance

Crouzon syndrome, Pfeiffer syndrome, craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis
Probe Type

Amplification/Deletion
Sizes

5; 10; 20 tests
Synonyms

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