Apert Syndrome - FGFR2 Exon 8
Molecular Test Requisition | Specimen Information | Billing Information | Contact Us | CPT Codes | Print Page APERT SYNDROME - FGFR2 EXON 8 Gene Symbol: FGFR2 (exon 8 only) Chromosomal Locus: 10q26 Protein: Fibroblast growth factor receptor 2