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#101600 - PFEIFFER SYNDROME
CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED
Cytogenetic locations: 17120318
Gene summaries Genetic tests Medical literature
#101400 - SAETHRE-CHOTZEN SYNDROME; SCS
SAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED
Cytogenetic locations: Micall2
#101200 - APERT SYNDROME
APERT-CROUZON DISEASE, INCLUDED
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