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#615465 - HARTSFIELD SYNDROME; HRTFDS
Cytogenetic locations: 609722
Gene summaries Genetic tests Medical literature
#613001 - ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL
#190440 - TRIGONOCEPHALY 1; TRIGNO1
Cytogenetic locations: 607359
#166250 - OSTEOGLOPHONIC DYSPLASIA; OGD
#147950 - HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA; HH2
Cytogenetic locations: 30698671
*136350 - FIBROBLAST GROWTH FACTOR RECEPTOR 1; FGFR1
FGFR1/BCR FUSION GENE, INCLUDED
#123150 - JACKSON-WEISS SYNDROME; JWS
Cytogenetic locations: 1p36, 607359
#101600 - PFEIFFER SYNDROME
CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED
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