Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss-Reference-Cited by-同舟云学术

Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss

Published:2022-12-14 Issue: Volume: Page:
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:The Laryngoscope

Author:

Perry Julia¹^ORCID,Redfield Shelby¹^ORCID,Oza Andrea¹²,Rouse Stephanie¹,Stewart Candace¹^ORCID,Khela Harmon¹,Srinivasan Tarika¹³,Albano Victoria¹,Shearer Eliot¹³^ORCID,Kenna Margaret¹³^ORCID

Affiliation:

1. Department of Otolaryngology and Communication Enhancement Boston Children's Hospital Boston Massachusetts USA

2. Clinical Genomics Invitae San Francisco California USA

3. Department of Otolaryngology‐Head and Neck Surgery Harvard Medical School Boston Massachusetts USA

Funder

National Institute on Deafness and Other Communication Disorders

Publisher

Wiley

Subject

Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/lary.30507

Reference33 articles.

1. Massively parallel sequencing for genetic diagnosis of hearing loss: the new standard of care;Shearer AE;Otolaryngol Head Neck Surg,2015

2. Racial and ethnic disparities in genetic testing for hearing loss: a systematic review and synthesis

3. Exome sequencing in infants with congenital hearing impairment: a population-based cohort study

4. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss

5. Reanalysis of Clinical Exome Sequencing Data

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