A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis

Exome sequencing (ES) has become one of the important diagnostic tools in clinical genetics with a reported diagnostic rate of 25–58%. Many studies have illustrated the diagnostic and immediate clinical impact of ES. However, up to 75% of individuals remain undiagnosed and there is scarce evidence s...

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Detalles Bibliográficos
Autores principales: Fung, Jasmine L. F., Yu, Mullin H. C., Huang, Shushu, Chung, Claudia C. Y., Chan, Marcus C. Y., Pajusalu, Sander, Mak, Christopher C. Y., Hui, Vivian C. C., Tsang, Mandy H. Y., Yeung, Kit San, Lek, Monkol, Chung, Brian H. Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484757/
https://www.ncbi.nlm.nih.gov/pubmed/32963807
http://dx.doi.org/10.1038/s41525-020-00144-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484757/
https://www.ncbi.nlm.nih.gov/pubmed/32963807
http://dx.doi.org/10.1038/s41525-020-00144-x

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