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Guidelines

Guidelines for aetiological investigation into severe to profound bilateral permanent childhood hearing impairment

Produced by the British Association of Audiovestibular Physicians (BAAP) (Appendix 5) 2015

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Rajeev Mathew, Fernando Rodriguez Bajo, Nicola Hatton, Louise Buttfield, Shravan Gowrishankar, Deborah Vickers, Neil Donnelly, James Tysome, Manohar Bance & Patrick Axon. (2021) Assessment of the cochlear implant pathway for newborn hearing screening referrals. Cochlear Implants International 22:6, pages 345-352.
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Maria Toms, Waheeda Pagarkar & Mariya Moosajee. (2020) Usher syndrome: clinical features, molecular genetics and advancing therapeutics. Therapeutic Advances in Ophthalmology 12, pages 251584142095219.
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Valerie Sung, Lilian Downie, Georgia A Paxton, Karen Liddle, Catherine S Birman, Wei Wei Chan, Carolyn Cottier, Alison Harris, Matthew Hunter, Elizabeth Peadon, Kenneth Peacock, Laurence Roddick, Elizabeth Rose, Kerryn Saunders & David J Amor. (2019) Childhood Hearing Australasian Medical Professionals network: Consensus guidelines on investigation and clinical management of childhood hearing loss. Journal of Paediatrics and Child Health 55:9, pages 1013-1022.
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Ladan Sadeghian, Mohammad Amin Tabatabaiefar, Najmeh Fattahi, Mohammad Reza Pourreza, Parisa Tahmasebi, Zahra Alavi & Morteza Hashemzadeh Chaleshtori. (2019) Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. International Journal of Pediatric Otorhinolaryngology 124, pages 99-105.
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