4 research outputs found
The diagnostic utility of clinical exome sequencing in 60 patients with hearing loss disorders:A single-institution experience
Get PDFPersonalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders
Get PDFThe diagnostic utility of clinical exome sequencing in 60 patients with hearing loss disorders: A single‐institution experience
Get PDFFrom Wiley via Jisc Publications RouterHistory: received 2020-12-21, rev-recd 2021-04-08, accepted 2021-05-08, pub-electronic 2021-07-05Article version: VoRPublication status: PublishedFunder: Mexico’s National Council of Science and Technology; Grant(s): (CONACyT)‐392996Funder: Peter Mount award (Manchester University NHS Foundation Trust); Grant(s): G70658Funder: Data Driven Award (Manchester University NHS Foundation Trust); Grant(s): NH_SY_020419Funder: Manchester NIHR BRC; Grant(s): BRC‐1215‐20007Funder: Wellcome Trust; Grant(s): 200990/Z/16/
