MeSH Browser

MeSH Supplementary: Robinow syndrome, autosomal recessive
Unique ID: C535863
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535863
Registry Numbers: 0
Heading Mapped to: Spine / abnormalities; *Limb Deformities, Congenital; *Maxillofacial Abnormalities
Frequency: 7
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Robinow syndrome, autosomal recessive MeSH Supplementary Concept Data 2025