The diagnostic utility of clinical exome sequencing in 60 patients with hearing loss disorders: A single-institution experience

Clin Otolaryngol. 2021 Nov;46(6):1257-1262. doi: 10.1111/coa.13826. Epub 2021 Jul 5.

Leslie P Molina-Ramírez^{1

2}, Emma Mm Burkitt-Wright^{1

2}, Haroon Saeed³, John H McDermott^{1

2}, Claire Kyle², Ronnie Wright², Christopher Campbell², Sanjeev S Bhaskar², Algy Taylor², Laura Dutton², Claire Forde², Kay Metcalfe^{1

2}, Audrey Smith^{1

2}, Jill Clayton-Smith^{1

2}, Sofia Douzgou^{1

2}, Kate Chandler^{1

2}, Tracy A Briggs^{1

2}, Siddharth Banka^{1

2}, William G Newman^{1

2}, David Gokhale², Iain A Bruce^{3

4}, Graeme C Black^{1

2}

¹ Division of Evolution and Genomic Sciences, Manchester Academic Health Science Centre, Faculty of Biology, Medicine and Health, School of Biological Sciences, University of Manchester, Manchester, UK.
² Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
³ Paediatric ENT Department, Manchester Academic Health Science Centre, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
⁴ Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine, Health University of Manchester, Manchester, UK.

No abstract available

Keywords: genomics; hearing loss; precision medicine.

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