MeSH Browser

MeSH Supplementary: X chromosome, monosomy Xp22 pter
Unique ID: C536754
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536754
Entry Term(s): Deletion Xp22 pter; Monosomy Xp22 pter
Registry Numbers: 0
Heading Mapped to: *Chromosome Deletion; *Sex Chromosome Aberrations; Chromosomes, Human, X
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

X chromosome, monosomy Xp22 pter MeSH Supplementary Concept Data 2025