Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years.
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| Title: | Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years. |
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| Authors: | Kernohan KD, Gallagher L, Pigeon M, Yeh E, Lacaria M, Axford MM, MacCormick J, Papaioannou V, Quercia N, Rupar C, Zimmerman K, Weber S, Cushing SL, Chakraborty P |
| Source: | Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2025 Oct; Vol. 27 (10), pp. 101497. Date of Electronic Publication: 2025 Sep 07. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40923571 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Kernohan+KD%22">Kernohan KD</searchLink><br /><searchLink fieldCode="AU" term="%22Gallagher+L%22">Gallagher L</searchLink><br /><searchLink fieldCode="AU" term="%22Pigeon+M%22">Pigeon M</searchLink><br /><searchLink fieldCode="AU" term="%22Yeh+E%22">Yeh E</searchLink><br /><searchLink fieldCode="AU" term="%22Lacaria+M%22">Lacaria M</searchLink><br /><searchLink fieldCode="AU" term="%22Axford+MM%22">Axford MM</searchLink><br /><searchLink fieldCode="AU" term="%22MacCormick+J%22">MacCormick J</searchLink><br /><searchLink fieldCode="AU" term="%22Papaioannou+V%22">Papaioannou V</searchLink><br /><searchLink fieldCode="AU" term="%22Quercia+N%22">Quercia N</searchLink><br /><searchLink fieldCode="AU" term="%22Rupar+C%22">Rupar C</searchLink><br /><searchLink fieldCode="AU" term="%22Zimmerman+K%22">Zimmerman K</searchLink><br /><searchLink fieldCode="AU" term="%22Weber+S%22">Weber S</searchLink><br /><searchLink fieldCode="AU" term="%22Cushing+SL%22">Cushing SL</searchLink><br /><searchLink fieldCode="AU" term="%22Chakraborty+P%22">Chakraborty P</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229815831%22">Genetics in medicine : official journal of the American College of Medical Genetics</searchLink> [Genet Med] 2025 Oct; Vol. 27 (10), pp. 101497. <i>Date of Electronic Publication: </i>2025 Sep 07. – Name: TypePub Label: Publication Type Group: TypPub Data: Published Erratum – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9815831 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1530-0366 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210983600%22">10983600 </searchLink><i>NLM ISO Abbreviation: </i>Genet Med <i>Subsets: </i>MEDLINE; In Process |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40923571 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.gim.2025.101497 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 101497 Titles: – TitleFull: Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kernohan KD – PersonEntity: Name: NameFull: Gallagher L – PersonEntity: Name: NameFull: Pigeon M – PersonEntity: Name: NameFull: Yeh E – PersonEntity: Name: NameFull: Lacaria M – PersonEntity: Name: NameFull: Axford MM – PersonEntity: Name: NameFull: MacCormick J – PersonEntity: Name: NameFull: Papaioannou V – PersonEntity: Name: NameFull: Quercia N – PersonEntity: Name: NameFull: Rupar C – PersonEntity: Name: NameFull: Zimmerman K – PersonEntity: Name: NameFull: Weber S – PersonEntity: Name: NameFull: Cushing SL – PersonEntity: Name: NameFull: Chakraborty P IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: 2025 Oct Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1530-0366 Numbering: – Type: volume Value: 27 – Type: issue Value: 10 Titles: – TitleFull: Genetics in medicine : official journal of the American College of Medical Genetics Type: main |
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