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ferritin, light polypeptide:
FTL
ferrochelatase (protoporphyria):
FECH
fibrillin 1:
FBN1
fibrillin 2 (congenital contractural arachnodactyly):
FBN2
fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome):
FGFR1
fibroblast growth factor receptor 2 (bacteria-expressed kinase, keratinocyte growth factor receptor, craniofacial dysostosis 1, Crouzon syndrome, Pfeiffer syndrome, Jackson-Weiss syndrome):
FGFR2
fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism):
FGFR3
fibroblast growth factor receptor 4:
FGFR4
fibroblast growth factor receptor-like 1:
FGFRL1
filamin A, alpha (actin binding protein 280):
FLNA
flavin containing monooxygenase 3:
FMO3
fms-related tyrosine kinase 4:
FLT4
folliculin:
FLCN
forkhead box C2 (MFH-1, mesenchyme forkhead 1):
FOXC2
forkhead box L2:
FOXL2
forkhead box P3:
FOXP3
fragile X mental retardation 1:
FMR1
frataxin:
FXN
fucosidase, alpha-L- 1, tissue:
FUCA1
fukutin:
FKTN
fumarate hydratase:
FH
fumarylacetoacetate hydrolase (fumarylacetoacetase):
FAH
FYVE, RhoGEF and PH domain containing 1:
FGD1
Published: January 23, 2009
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