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Article

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

BioMed research international - 1 Jan 2016

Ho Karen S, Twede Hope, Vanzo Rena, Harward Erin, Hensel Charles H, Martin Megan M, Page Stephanie, Peiffer Andreas, Mowery-Rushton Patricia, Serrano Moises, Wassman E Robert

Abstract excerpt

Copy number variants (CNVs) as detected by chromosomal microarray analysis (CMA) significantly contribute to the etiology of neurodevelopmental disorders, such as developmental delay (DD), intellectual disability (ID), and autism spectrum disorder (ASD). This study summarizes the results of 3.5 years of CMA testing by a CLIA-certified clinical testing laboratory 5487 patients with neurodevelopmental conditions...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 27975050
DOI: 10.1155/2016/3284534
PMCID: PMC5128689

Provenance

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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