Chromosome 16p13.3 Deletion Syndrome MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Chromosome 16p13.3 Deletion Syndrome
Unique ID: C566433
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566433
Entry Term(s): RSTS, Severe; Rubinstein-Taybi Syndrome, Severe
Registry Number: 0
Heading Mapped to: Chromosomes, Human, Pair 16; *Rubinstein-Taybi Syndrome
Frequency: 2
Date of Entry: 2012/11/05

Chromosome 16p13.3 Deletion Syndrome Preferred

page delivered in 0.004s