Chromosome 17p13.3 Duplication Syndrome MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Chromosome 17p13.3 Duplication Syndrome
Unique ID: C567705
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567705
Heading Mapped to: *Developmental Disabilities; *Nervous System Malformations; *Chromosome Disorders; *Chromosome Duplication
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chromosome 17p13.3 Duplication Syndrome Preferred

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