The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population.
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| Title: | The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population. |
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| Authors: | Khalaf T; Genetic Counseling Division, Igenomix, Dubai, UAE., Al Ojaimi M; Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, UAE.; Department of Pediatrics, University Hospital Sharjah, Sharjah, UAE., Saleh DA; Pediatric Neurology Division, American Center for Psychiatry and Neurology, Abu Dhabi, UAE.; Department of Pediatrics, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Sulaiman A; Pediatric Division, KidsHeart Medical Center, Abu Dhabi, UAE., Sohal AP; Pediatric Neurology Division, Neuropedia Children's Neuroscience Center, Dubai, UAE.; Pediatric Neurology Division, Al Qassimi Women and Children's Hospital, Sharjah, UAE., Khan A; Pediatric Neurology Division, Neuropedia Children's Neuroscience Center, Dubai, UAE.; Pediatric Division, Kings College Hospital London, Dubai, UAE.; Pediatric Neurology Division, Kids Neuro Clinic and Rehab Center, Dubai, UAE., El-Hattab AW; Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, UAE.; Department of Pediatrics, University Hospital Sharjah, Sharjah, UAE. |
| Source: | Clinical genetics [Clin Genet] 2024 Jul; Vol. 106 (1), pp. 82-89. Date of Electronic Publication: 2024 Mar 04. |
| 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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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 38438125 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Khalaf+T%22">Khalaf T</searchLink>; Genetic Counseling Division, Igenomix, Dubai, UAE.<br /><searchLink fieldCode="AU" term="%22Al+Ojaimi+M%22">Al Ojaimi M</searchLink>; Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, UAE.; Department of Pediatrics, University Hospital Sharjah, Sharjah, UAE.<br /><searchLink fieldCode="AU" term="%22Saleh+DA%22">Saleh DA</searchLink>; Pediatric Neurology Division, American Center for Psychiatry and Neurology, Abu Dhabi, UAE.; Department of Pediatrics, Faculty of Medicine, Ain Shams University, Cairo, Egypt.<br /><searchLink fieldCode="AU" term="%22Sulaiman+A%22">Sulaiman A</searchLink>; Pediatric Division, KidsHeart Medical Center, Abu Dhabi, UAE.<br /><searchLink fieldCode="AU" term="%22Sohal+AP%22">Sohal AP</searchLink>; Pediatric Neurology Division, Neuropedia Children's Neuroscience Center, Dubai, UAE.; Pediatric Neurology Division, Al Qassimi Women and Children's Hospital, Sharjah, UAE.<br /><searchLink fieldCode="AU" term="%22Khan+A%22">Khan A</searchLink>; Pediatric Neurology Division, Neuropedia Children's Neuroscience Center, Dubai, UAE.; Pediatric Division, Kings College Hospital London, Dubai, UAE.; Pediatric Neurology Division, Kids Neuro Clinic and Rehab Center, Dubai, UAE.<br /><searchLink fieldCode="AU" term="%22El-Hattab+AW%22">El-Hattab AW</searchLink>; Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, UAE.; Department of Pediatrics, University Hospital Sharjah, Sharjah, UAE. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2024 Jul; Vol. 106 (1), pp. 82-89. <i>Date of Electronic Publication: </i>2024 Mar 04. – 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=38438125 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.14508 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 82 Titles: – TitleFull: The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Khalaf T – PersonEntity: Name: NameFull: Al Ojaimi M – PersonEntity: Name: NameFull: Saleh DA – PersonEntity: Name: NameFull: Sulaiman A – PersonEntity: Name: NameFull: Sohal AP – PersonEntity: Name: NameFull: Khan A – PersonEntity: Name: NameFull: El-Hattab AW IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 07 Text: 2024 Jul Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1399-0004 Numbering: – Type: volume Value: 106 – Type: issue Value: 1 Titles: – TitleFull: Clinical genetics Type: main |
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