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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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| Pubblicato in: | J Community Genet |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer Berlin Heidelberg
2015
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| Soggetti: | |
| Accesso online: | 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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