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Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss

Crossref DOI link: https://doi.org/10.1038/s41436-018-0004-x

Published Print: 2018-12

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Sheppard, Sarah

Biswas, Sawona

Li, Mindy H.

Jayaraman, Vijayakumar

Slack, Ian

Romasko, Edward J.

Sasson, Ariella

Brunton, Joshua

Rajagopalan, Ramakrishnan

Sarmady, Mahdi

Abrudan, Jenica L.

Jairam, Sowmya

DeChene, Elizabeth T.

Ying, Xiahoan

Choi, Jiwon

Wilkens, Alisha

Raible, Sarah E.

Scarano, Maria I.

Santani, Avni

Pennington, Jeffrey W.

Luo, Minjie

Conlin, Laura K.

Devkota, Batsal

Dulik, Matthew C.

Spinner, Nancy B.

Krantz, Ian D.
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Text and Data Mining valid from 2018-12-01

Text and Data Mining valid from 2018-12-01

Version of Record valid from 2021-11-24
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This article is maintained by: Elsevier

Article Title: Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0004-x

Content Type: article

Copyright: © 2018, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics