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

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery - 1 Nov 2021

Molina-Ramírez Leslie P, Burkitt-Wright Emma Mm, Saeed Haroon, McDermott John H, Kyle Claire, Wright Ronnie, Campbell Christopher, Bhaskar Sanjeev S, Taylor Algy, Dutton Laura, Forde Claire, Metcalfe Kay, Smith Audrey, Clayton-Smith Jill, Douzgou Sofia, Chandler Kate, Briggs Tracy A, Banka Siddharth, Newman William G, Gokhale David, Bruce Iain A, Black Graeme C

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 34171171
DOI: 10.1111/coa.13826

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis.Semantic proximity Read ↗

Molecular diagnosis of non-syndromic hearing loss patients using a stepwise approach.Semantic proximity Read ↗

Next-generation sequence testing expands research into causes of hearing loss: scientists examine role of multiple mutations in individual cases.Semantic proximity Read ↗

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.Semantic proximity Read ↗

Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.Semantic proximity Read ↗

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