MeSH Browser

MeSH Supplementary: X chromosome, trisomy Xp3
Unique ID: C536756
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536756
Entry Term(s): Duplication Xp3; Trisomy Xp3
Heading Mapped to: *Sex Chromosome Aberrations; *Trisomy; Chromosomes, Human, X
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

X chromosome, trisomy Xp3 MeSH Supplementary Concept Data 2024