MeSH Browser

MeSH Supplementary: Chromosome 15q26-Qter Deletion Syndrome
Unique ID: C567232
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567232
Entry Term(s): Drayer Syndrome
Heading Mapped to: *Abnormalities, Multiple; *Growth Disorders; *Intellectual Disability; *Microcephaly
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome 15q26-Qter Deletion Syndrome MeSH Supplementary Concept Data 2024