Correspondence to Hale et al. atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria.
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| Title: | Correspondence to Hale et al. atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria. |
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| Authors: | Blake K; Department of Pediatrics, IWK Health Center, Dalhousie University, Nova Scotia, Canada., Trider CL; Department of Pediatrics, Kingston General Hospital, Queen's University, Ontario, Canada., Hartshorne TS; Department of Psychology, Central Michigan University, Mount Pleasant, Michigan., Stratton KK; Department of Counseling, Educational Psychology, and Foundations, Mississippi State University, Starkville, Mississippi. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2016 Dec; Vol. 170 (12), pp. 3365-3366. Date of Electronic Publication: 2016 Oct 14. |
| Publication Type: | Letter |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 27739643 AccessLevel: 2 PubType: Editorial & Opinion PubTypeId: editorialOpinion PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Correspondence to Hale et al. atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Blake+K%22">Blake K</searchLink>; Department of Pediatrics, IWK Health Center, Dalhousie University, Nova Scotia, Canada.<br /><searchLink fieldCode="AU" term="%22Trider+CL%22">Trider CL</searchLink>; Department of Pediatrics, Kingston General Hospital, Queen's University, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Hartshorne+TS%22">Hartshorne TS</searchLink>; Department of Psychology, Central Michigan University, Mount Pleasant, Michigan.<br /><searchLink fieldCode="AU" term="%22Stratton+KK%22">Stratton KK</searchLink>; Department of Counseling, Educational Psychology, and Foundations, Mississippi State University, Starkville, Mississippi. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2016 Dec; Vol. 170 (12), pp. 3365-3366. <i>Date of Electronic Publication: </i>2016 Oct 14. – Name: TypePub Label: Publication Type Group: TypPub Data: Letter – Name: TitleSource Label: Journal Info Group: Src 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>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=27739643 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.37627 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3365 Titles: – TitleFull: Correspondence to Hale et al. atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Blake K – PersonEntity: Name: NameFull: Trider CL – PersonEntity: Name: NameFull: Hartshorne TS – PersonEntity: Name: NameFull: Stratton KK IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2016 Dec Type: published Y: 2016 Identifiers: – Type: issn-electronic Value: 1552-4833 Numbering: – Type: volume Value: 170 – Type: issue Value: 12 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
| ResultId | 1 |
