Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results

PURPOSE: Detection of all major classes of genomic variants in a single test would decrease cost and increase the efficiency of genomic diagnostics. Genome sequencing (GS) has the potential to provide this level of comprehensive detection. We sought to demonstrate the utility of GS in the molecular...

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Bibliographic Details
Published in:Genet Med
Main Authors: Rajagopalan, Ramakrishnan, Gilbert, Melissa A., McEldrew, Deborah A., Nassur, James A., Loomes, Kathleen M., Piccoli, David A., Krantz, Ian D., Conlin, Laura K., Spinner, Nancy B.
Format: Artigo
Language:Inglês
Published: Nature Publishing Group US 2020
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7862053/
https://ncbi.nlm.nih.gov/pubmed/33077891
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-020-00989-8
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