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SAETHRE-CHOTZEN SYNDROME
BEK, MOUSE, HOMOLOG OF
BEARE-STEVENSON CUTIS GYRATA SYNDROME
KGFR
PFEIFFER SYNDROME, TYPE III
APERT SYNDROME
GASTRIC CANCER, SOMATIC
CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT
KERATINOCYTE GROWTH FACTOR RECEPTOR
PFEIFFER SYNDROME VARIANT
BENT BONE DYSPLASIA SYNDROME 1
ENDOMETRIAL CANCER, SOMATIC
FGF RECEPTOR
CROUZON SYNDROME
PFEIFFER SYNDROME
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS
SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND IMPAIRED INTELLECTUAL DEVELOPMENT
FIBROBLAST GROWTH FACTOR RECEPTOR BEK
TK14
CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA
PROTEIN TYROSINE KINASE, RECEPTOR-LIKE, 14
LADD SYNDROME 1
CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL
JACKSON-WEISS SYNDROME
FGFR2
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