MeSH Browser

MeSH Supplementary: Chromosome 11p Deletion Syndrome
Unique ID: C541598
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C541598
Entry Term(s): 11p Deletion Syndrome
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 11; *WAGR Syndrome
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Chromosome 11p Deletion Syndrome MeSH Supplementary Concept Data 2025