MeSH Browser

MeSH Supplementary: Chromosome 10q26 Deletion Syndrome
Unique ID: C567182
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567182
Entry Term(s): Terminal Chromosome 10q26 Deletion Syndrome
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 10; *Learning Disabilities; *Facies
Frequency: 6
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome 10q26 Deletion Syndrome MeSH Supplementary Concept Data 2025