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.
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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ISSN:1399-0004
DOI:10.1111/cge.14508