MeSH Browser

MeSH Supplementary: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Unique ID: C566604
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566604
Registry Number: 0
Heading Mapped to: Cornea / *abnormalities; *Heart Defects, Congenital; *Hearing Loss
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Deafness, Congenital Heart Defects, and Posterior Embryotoxon MeSH Supplementary Concept Data 2023