Mutation of this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Chromosomal ab

The FGFR1/CSP8 FISH Probe is intended for use to qualitatively detect the FGFR1 gene amplification/deletion via fluorescence in situ hybridization