MeSH Browser

MeSH Supplementary: Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
Unique ID: C567291
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567291
Entry Term(s): 1q21.1 Contiguous Gene Deletion; 1q21.1 Deletion; 1q21.1 Microdeletion; Chromosome 1q21.1 Deletion Syndrome
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Chromosome Deletion; Chromosomes, Human, Pair 1; *Megalencephaly
Frequency: 21
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb MeSH Supplementary Concept Data 2025