Chromosome 2p16.1-P15 Deletion Syndrome MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Chromosome 2p16.1-P15 Deletion Syndrome
Unique ID: C567289
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567289
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; *Chromosome Deletion; Chromosomes, Human, Pair 2; *Craniofacial Abnormalities
Frequency: 1
Date of Entry: 2012/11/05

Chromosome 2p16.1-P15 Deletion Syndrome Preferred

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