MeSH Browser

MeSH Supplementary: X chromosome, trisomy Xpter Xq13
Unique ID: C536731
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536731
Entry Term(s): Duplication Xpter Xq13; Trisomy Xpter Xq13
Registry Numbers: 0
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 Xpter Xq13 MeSH Supplementary Concept Data 2025