Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
#614592 - BENT BONE DYSPLASIA SYNDROME 1; BBDS1
Cytogenetic locations: 22387015
Gene summaries Genetic tests Medical literature
#613659 - GASTRIC CANCER
GASTRIC CANCER, INTESTINAL, INCLUDED
Cytogenetic locations: 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 1p36, 609523, 1p36, 12p13.31
#609579 - SCAPHOCEPHALY, MAXILLARY RETRUSION, AND IMPAIRED INTELLECTUAL DEVELOPMENT
#207410 - ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS; ABS2
Cytogenetic locations: 617462
*176943 - FIBROBLAST GROWTH FACTOR RECEPTOR 2; FGFR2
KERATINOCYTE GROWTH FACTOR RECEPTOR, INCLUDED; KGFR, INCLUDED
Cytogenetic locations: 15523615
#149730 - LACRIMOAURICULODENTODIGITAL SYNDROME 1; LADD1
Cytogenetic locations: 13709571
#123790 - BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS
#123500 - CROUZON SYNDROME
#123150 - JACKSON-WEISS SYNDROME; JWS
Cytogenetic locations: 1p36, 607359
#101600 - PFEIFFER SYNDROME
CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED
Cytogenetic locations: 609722
#101400 - SAETHRE-CHOTZEN SYNDROME; SCS
SAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED
Cytogenetic locations: 19792855
#101200 - APERT SYNDROME
APERT-CROUZON DISEASE, INCLUDED
Filter your results:
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on