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