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Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort.

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Title: Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort.
Authors: Wener ER; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada., McLennan JD; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada., Papsin BC; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Otolaryngology-Head and Neck Surgery, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada., Cushing SL; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Otolaryngology-Head and Neck Surgery, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada., Stavropoulos DJ; Genome Diagnostics Paediatric Laboratory Medicine, Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada., Mendoza-Londono R; Genome Diagnostics Paediatric Laboratory Medicine, Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada., Quercia N; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada., Gordon KA; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Otolaryngology-Head and Neck Surgery, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada.
Source: The Laryngoscope [Laryngoscope] 2024 Aug; Vol. 134 (8), pp. 3832-3838. Date of Electronic Publication: 2024 Mar 01.
Publication Type: Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 8607378 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-4995 (Electronic) Linking ISSN: 0023852X NLM ISO Abbreviation: Laryngoscope Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Variants in Genes Associated with Hearing Loss in Children: Prevalence in a Large Canadian Cohort.
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  Data: <searchLink fieldCode="AU" term="%22Wener+ER%22">Wener ER</searchLink>; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22McLennan+JD%22">McLennan JD</searchLink>; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Papsin+BC%22">Papsin BC</searchLink>; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Otolaryngology-Head and Neck Surgery, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Cushing+SL%22">Cushing SL</searchLink>; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Otolaryngology-Head and Neck Surgery, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Stavropoulos+DJ%22">Stavropoulos DJ</searchLink>; Genome Diagnostics Paediatric Laboratory Medicine, Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Mendoza-Londono+R%22">Mendoza-Londono R</searchLink>; Genome Diagnostics Paediatric Laboratory Medicine, Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Quercia+N%22">Quercia N</searchLink>; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Gordon+KA%22">Gordon KA</searchLink>; Archie's Cochlear Implant Laboratory, Neuroscience & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Otolaryngology-Head and Neck Surgery, University of Toronto, Hospital for Sick Children, Toronto, Ontario, Canada.
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  Data: <searchLink fieldCode="JN" term="%228607378%22">The Laryngoscope</searchLink> [Laryngoscope] 2024 Aug; Vol. 134 (8), pp. 3832-3838. <i>Date of Electronic Publication: </i>2024 Mar 01.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8607378 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1531-4995 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220023852X%22">0023852X </searchLink><i>NLM ISO Abbreviation: </i>Laryngoscope <i>Subsets: </i>MEDLINE
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        Value: 10.1002/lary.31373
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        Text: English
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              M: 08
              Text: 2024 Aug
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              Y: 2024
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