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Article

The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.

Clinical genetics - 1 Sept 2014

Christenhusz G M, Devriendt K, Peeters H, Van Esch H, Dierickx K

Abstract excerpt

Children with unexplained developmental disabilities or congenital anomalies are increasingly being referred for genetic diagnostic testing using array-comparative genomic hybridisation (array-CGH) and next-generation sequencing (NGS) technologies. Their parents will have to deal with the secondary variants that will inevitably arise. We conducted 16 prospective semi-structured interviews with native...

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PMID: 24479378
DOI: 10.1111/cge.12354

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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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