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Article

Clinical characterization of novel chromosome 22q13 microdeletions.

International journal of pediatric otorhinolaryngology - 1 Apr 2017

Ha Jennifer F, Ahmad Ayesha, Lesperance Marci M

Abstract excerpt

INTRODUCTION: The advent of chromosome microarray analysis (CMA) for evaluation of patients with multiple congenital anomalies has made it possible to define chromosomal imbalances with greater precision and resolutions significantly smaller than possible by standard G-banded chromosome analysis. We describe two patients with novel chromosomal anomalies involving chromosome 22q13, a locus also associated with...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28576520
DOI: 10.1016/j.ijporl.2016.12.008

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ABR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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