- OMIM ID
-
610543
- OMIM term:
- CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL
- Alternative terms:
-
RUBINSTEIN-TAYBI DELETION SYNDROME
RSTS DELETION SYNDROME
- (∗) Location:
- 16p13.3
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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