Dual Diagnosis of Nongoitrous Congenital Hypothyroidism-6 and Snijders Blok-Campeau Syndrome.
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| Title: | Dual Diagnosis of Nongoitrous Congenital Hypothyroidism-6 and Snijders Blok-Campeau Syndrome. |
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| Authors: | Yalçın HY; Department of Pediatric Genetics, Tepecik Education and Research Hospital, Izmir, Turkey., Cinleti T; Department of Pediatric Genetics, Tepecik Education and Research Hospital, Izmir, Turkey., Yel S; Department of Pediatric Endocrinology, Van Training and Research Hospital, Van, Turkey., Mutlu MB; Department of Genetics, Deta Gen Genetic Diseases Diagnosis Center, Kayseri, Turkey. |
| Source: | Molecular syndromology [Mol Syndromol] 2024 Jun; Vol. 15 (3), pp. 240-246. Date of Electronic Publication: 2024 Jan 24. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not 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: 38841327 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Dual Diagnosis of Nongoitrous Congenital Hypothyroidism-6 and Snijders Blok-Campeau Syndrome. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Yalçın+HY%22">Yalçın HY</searchLink>; Department of Pediatric Genetics, Tepecik Education and Research Hospital, Izmir, Turkey.<br /><searchLink fieldCode="AU" term="%22Cinleti+T%22">Cinleti T</searchLink>; Department of Pediatric Genetics, Tepecik Education and Research Hospital, Izmir, Turkey.<br /><searchLink fieldCode="AU" term="%22Yel+S%22">Yel S</searchLink>; Department of Pediatric Endocrinology, Van Training and Research Hospital, Van, Turkey.<br /><searchLink fieldCode="AU" term="%22Mutlu+MB%22">Mutlu MB</searchLink>; Department of Genetics, Deta Gen Genetic Diseases Diagnosis Center, Kayseri, Turkey. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101525192%22">Molecular syndromology</searchLink> [Mol Syndromol] 2024 Jun; Vol. 15 (3), pp. 240-246. <i>Date of Electronic Publication: </i>2024 Jan 24. – 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="%22S%2E+Karger%22">S. Karger </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101525192 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>1661-8769 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216618769%22">16618769 </searchLink><i>NLM ISO Abbreviation: </i>Mol Syndromol <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=38841327 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1159/000535682 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 240 Titles: – TitleFull: Dual Diagnosis of Nongoitrous Congenital Hypothyroidism-6 and Snijders Blok-Campeau Syndrome. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yalçın HY – PersonEntity: Name: NameFull: Cinleti T – PersonEntity: Name: NameFull: Yel S – PersonEntity: Name: NameFull: Mutlu MB IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: 2024 Jun Type: published Y: 2024 Identifiers: – Type: issn-print Value: 1661-8769 Numbering: – Type: volume Value: 15 – Type: issue Value: 3 Titles: – TitleFull: Molecular syndromology Type: main |
| ResultId | 1 |
