Chromosome 1q21.1 Duplication Syndrome MeSH Supplementary Concept Data 2026

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Concepts

MeSH Supplementary: Chromosome 1q21.1 Duplication Syndrome
Unique ID: C567290
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567290
Registry Numbers: 0
Heading Mapped to: Autistic Disorder; *Chromosome Deletion; Chromosomes, Human, Pair 1; *Heart Defects, Congenital; *Intellectual Disability
Frequency: 1
Date Introduced: 2012/11/05
Last Updated: 2012/11/05

Chromosome 1q21.1 Duplication Syndrome Preferred

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