MeSH Browser

MeSH Supplementary: Chromosome 22q11.2 Microduplication Syndrome
Unique ID: C567224
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567224
Entry Term(s): 22q11.2 Duplication; Chromosome 22q11.2 Duplication Syndrome
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; Chromosomes, Human, Pair 22; *DiGeorge Syndrome; *Chromosome Duplication
Frequency: 47
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Chromosome 22q11.2 Microduplication Syndrome MeSH Supplementary Concept Data 2024