Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus.
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| Title: | Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus. |
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| Authors: | Chan JCK; Department of Clinical Genetics, Hong Kong Children's Hospital, Hong Kong, China., Siu LLP, Ho SKL, Cheng SSW, Luk HM |
| Source: | Clinical dysmorphology [Clin Dysmorphol] 2025 Oct 01; Vol. 34 (4), pp. 142-146. Date of Electronic Publication: 2025 Jun 30. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40586236 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Chan+JCK%22">Chan JCK</searchLink>; Department of Clinical Genetics, Hong Kong Children's Hospital, Hong Kong, China.<br /><searchLink fieldCode="AU" term="%22Siu+LLP%22">Siu LLP</searchLink><br /><searchLink fieldCode="AU" term="%22Ho+SKL%22">Ho SKL</searchLink><br /><searchLink fieldCode="AU" term="%22Cheng+SSW%22">Cheng SSW</searchLink><br /><searchLink fieldCode="AU" term="%22Luk+HM%22">Luk HM</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229207893%22">Clinical dysmorphology</searchLink> [Clin Dysmorphol] 2025 Oct 01; Vol. 34 (4), pp. 142-146. <i>Date of Electronic Publication: </i>2025 Jun 30. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9207893 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1473-5717 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209628827%22">09628827 </searchLink><i>NLM ISO Abbreviation: </i>Clin Dysmorphol <i>Subsets: </i>MEDLINE; In Process |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40586236 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1097/MCD.0000000000000531 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 142 Titles: – TitleFull: Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Chan JCK – PersonEntity: Name: NameFull: Siu LLP – PersonEntity: Name: NameFull: Ho SKL – PersonEntity: Name: NameFull: Cheng SSW – PersonEntity: Name: NameFull: Luk HM IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: 2025 Oct 01 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1473-5717 Numbering: – Type: volume Value: 34 – Type: issue Value: 4 Titles: – TitleFull: Clinical dysmorphology Type: main |
| ResultId | 1 |
