Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy.
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| Title: | Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy. |
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| Authors: | David O; Pediatric Endocrinology Unit, Soroka University Medical Center, Beer-Sheva, Israel.; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel., Eskin-Schwartz M; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel., Ling G; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Pediatric Gastroenterology Unit, Soroka University Medical Center, Beer-Sheva, Israel., Dolgin V; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel., Kristal E; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel., Benkowitz E; Radiology Department, Soroka Medical Center, Beer-Sheva, Israel., Osyntsov L; Institute of Pathology, Soroka Medical Center, Beer-Sheva, Israel., Gradstein L; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Ophthalmology Clinic, Southern District, Clalit Health Services, Beer-sheva, Israel., Birk OS; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel., Loewenthal N; Pediatric Endocrinology Unit, Soroka University Medical Center, Beer-Sheva, Israel.; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel., Yerushalmi B; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Pediatric Gastroenterology Unit, Soroka University Medical Center, Beer-Sheva, Israel. |
| Source: | Clinical genetics [Clin Genet] 2020 Sep; Vol. 98 (3), pp. 303-307. Date of Electronic Publication: 2020 Aug 03. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 32617964 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22David+O%22">David O</searchLink>; Pediatric Endocrinology Unit, Soroka University Medical Center, Beer-Sheva, Israel.; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Eskin-Schwartz+M%22">Eskin-Schwartz M</searchLink>; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Ling+G%22">Ling G</searchLink>; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Pediatric Gastroenterology Unit, Soroka University Medical Center, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Dolgin+V%22">Dolgin V</searchLink>; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Kristal+E%22">Kristal E</searchLink>; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Benkowitz+E%22">Benkowitz E</searchLink>; Radiology Department, Soroka Medical Center, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Osyntsov+L%22">Osyntsov L</searchLink>; Institute of Pathology, Soroka Medical Center, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Gradstein+L%22">Gradstein L</searchLink>; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Ophthalmology Clinic, Southern District, Clalit Health Services, Beer-sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Birk+OS%22">Birk OS</searchLink>; Genetics Institute at Soroka University Medical Center and the Morris Kahn Laboratory of Human Genetics, National Center for Rare Diseases, at the Faculty of Health Sciences and National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Loewenthal+N%22">Loewenthal N</searchLink>; Pediatric Endocrinology Unit, Soroka University Medical Center, Beer-Sheva, Israel.; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.<br /><searchLink fieldCode="AU" term="%22Yerushalmi+B%22">Yerushalmi B</searchLink>; Saban Pediatric Medical Center for Israel, Soroka University Medical Center, Beer-Sheva, Israel.; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.; Pediatric Gastroenterology Unit, Soroka University Medical Center, Beer-Sheva, Israel. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2020 Sep; Vol. 98 (3), pp. 303-307. <i>Date of Electronic Publication: </i>2020 Aug 03. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32617964 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.13805 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 303 Titles: – TitleFull: Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: David O – PersonEntity: Name: NameFull: Eskin-Schwartz M – PersonEntity: Name: NameFull: Ling G – PersonEntity: Name: NameFull: Dolgin V – PersonEntity: Name: NameFull: Kristal E – PersonEntity: Name: NameFull: Benkowitz E – PersonEntity: Name: NameFull: Osyntsov L – PersonEntity: Name: NameFull: Gradstein L – PersonEntity: Name: NameFull: Birk OS – PersonEntity: Name: NameFull: Loewenthal N – PersonEntity: Name: NameFull: Yerushalmi B IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: 2020 Sep Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 1399-0004 Numbering: – Type: volume Value: 98 – Type: issue Value: 3 Titles: – TitleFull: Clinical genetics Type: main |
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