MeSH Browser

MeSH Supplementary: Chromosome 10q23 Deletion Syndrome
Unique ID: C567385
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567385
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 10; *Adenomatous Polyps
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome 10q23 Deletion Syndrome MeSH Supplementary Concept Data 2024