MeSH Browser

MeSH Supplementary: Cerebellar Granule Cell Hypertrophy and Megalencephaly
Unique ID: C563565
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563565
Heading Mapped to: *Hamartoma Syndrome, Multiple; *Malformations of Cortical Development, Group I
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2014/08/08

Cerebellar Granule Cell Hypertrophy and Megalencephaly MeSH Supplementary Concept Data 2024