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Variants of unknown significance on chromosomal microarray analysis: parental perspectives

Chromosomal microarray is the recommended first-tier genetic test when a child presents with idiopathic developmental delay (DD), intellectual disability (ID), and/or autism spectrum disorder (ASD). Microarray may discover variants of unknown clinical significance (VUS) and been suggested to cause p...

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Dades bibliogràfiques
Publicat a:J Community Genet
Autors principals: Jez, Stephanie, Martin, Megan, South, Sarah, Vanzo, Rena, Rothwell, Erin
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2015
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4567987/
https://ncbi.nlm.nih.gov/pubmed/25666435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12687-015-0218-4
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