Norman Roberts lissencephaly syndrome MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Norman Roberts lissencephaly syndrome
Unique ID: C537848
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537848
Entry Term(s): Lissencephaly 2; Lissencephaly syndrome, Norman-Roberts type
Heading Mapped to: *Lissencephaly
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Norman Roberts lissencephaly syndrome Preferred

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