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Article

A rare case of a de novo dup(19q) associated with a mild phenotype.

Journal of medical genetics - 1 Oct 2002

Qorri M, Oei P, Dockery H, McGaughran J

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Share to Chromosomes, Human, Pair 19
Share to Child, Preschool
Share to Developmental Disabilities
Share to Gene Duplication

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 12362043
DOI: 10.1136/jmg.39.10.e61
PMCID: PMC1734984

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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