MeSH Browser

MeSH Supplementary: Chromosome 19q13.11 Deletion Syndrome
Unique ID: C567810
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567810
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Chromosome Deletion; *Chromosome Disorders
Frequency: 1
Date of Entry: 2012/08/24
Revision Date: 1955/01/01

Chromosome 19q13.11 Deletion Syndrome MeSH Supplementary Concept Data 2025