Clinicians’ Views and Experiences with Offering and Returning Results from Exome Sequencing to Parents of Infants with Hearing Loss

Exome sequencing (ES) is an effective method for identifying the genetic cause of hearing loss in infants diagnosed through newborn hearing screening programs. ES has the potential to be integrated into routine clinical care, yet little is known about the experiences of clinicians offering this test...

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Detalles Bibliográficos
Autores principales: Notini, Lauren, Gaff, Clara L., Savulescu, Julian, Vears, Danya F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745321/
https://www.ncbi.nlm.nih.gov/pubmed/35011775
http://dx.doi.org/10.3390/jcm11010035

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745321/
https://www.ncbi.nlm.nih.gov/pubmed/35011775
http://dx.doi.org/10.3390/jcm11010035

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