MeSH Browser

MeSH Supplementary: Fragile Site 16p12
Unique ID: C565001
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565001
Registry Numbers: 0
Heading Mapped to: Mental Disorders; Developmental Disabilities; *Chromosome Deletion; Chromosomes, Human, Pair 16; *Heart Defects, Congenital; *Craniofacial Abnormalities; *Chromosome Disorders
Frequency: 3
Note: deletion = Chromomsome 16p12.1 Deletion Syndrome
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Fragile Site 16p12 MeSH Supplementary Concept Data 2025