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Phenotypic variability to medication management: an update on fragile X syndrome.
Elhawary, Nasser A; AlJahdali, Imad A; Abumansour, Iman S; Azher, Zohor A; Falemban, Alaa H; Madani, Wefaq M; Alosaimi, Wafaa; Alghamdi, Ghydda; Sindi, Ikhlas A.
Afiliación
  • Elhawary NA; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, Mecca, 21955, Saudi Arabia. naelhawary@uqu.edu.sa.
  • AlJahdali IA; Department of Community Medicine, College of Medicine, Umm Al-Qura University, Mecca, Saudi Arabia.
  • Abumansour IS; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, Mecca, 21955, Saudi Arabia.
  • Azher ZA; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, Mecca, 21955, Saudi Arabia.
  • Falemban AH; Department of Pharmacology and Toxicology, College of Medicine, Umm Al-Qura University, Mecca, 24382, Saudi Arabia.
  • Madani WM; Department of Hematology and Immunology, Faculty of Medicine, Umm Al-Qura University, Mecca, Saudi Arabia.
  • Alosaimi W; Department of Hematology, Maternity and Children Hospital, Mecca, Saudi Arabia.
  • Alghamdi G; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, Mecca, 21955, Saudi Arabia.
  • Sindi IA; Department of Biology, Faculty of Science, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.
Hum Genomics ; 17(1): 60, 2023 Jul 07.
Article en En | MEDLINE | ID: mdl-37420260
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno del Espectro Autista / Síndrome del Cromosoma X Frágil Tipo de estudio: Risk_factors_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno del Espectro Autista / Síndrome del Cromosoma X Frágil Tipo de estudio: Risk_factors_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita