MeSH Browser

MeSH Supplementary: X chromosome, duplication Xq13 1 q21 1
Unique ID: C536753
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536753
Entry Term(s): Duplication Xq13 1 q21 1; Trisomy Xq13 1 q21 1
Registry Number: 0
Heading Mapped to: *Sex Chromosome Aberrations; *Trisomy; Chromosomes, Human, X
Frequency: 4
Date of Entry: 2010/08/25

X chromosome, duplication Xq13 1 q21 1 MeSH Supplementary Concept Data 2024