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

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Veröffentlicht in:	Clinical otolaryngology 2021-11, Vol.46 (6), p.1257-1262
Hauptverfasser:	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.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Child Child, Preschool Female genomics Hearing loss Hearing Loss - genetics Humans Infant Male Middle Aged Mutation Phenotype precision medicine Retrospective Studies Surveys and Questionnaires Whole Exome Sequencing Young Adult
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