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Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
Chaudhary, Adeel G; Hussein, Ibtessam R; Abuzenadah, Adel; Gari, Mamdouh; Bassiouni, Randa; Sogaty, Samira; Lary, Sahira; Al-Quaiti, Maha; Al Balwi, Mohammed; Al Qahtani, Mohammed.
Afiliação
  • Chaudhary AG; Faculty of Medical Sciences, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
  • Hussein IR; Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia. Electronic address: irhussein@gmail.com.
  • Abuzenadah A; Faculty of Medical Sciences, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
  • Gari M; Faculty of Medical Sciences, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
  • Bassiouni R; Pediatric Hospital, Ministry of Health, Al Taif, Kingdom of Saudi Arabia.
  • Sogaty S; King Fahd Hospital, Jeddah, Kingdom of Saudi Arabia.
  • Lary S; Faculty of Science, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
  • Al-Quaiti M; Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
  • Al Balwi M; King Abdulaziz Medical City for National Guard Health Affairs, and King Saud bin Abdulaziz University for Health Sciences, Riyadh, Kingdom of Saudi Arabia.
  • Al Qahtani M; Faculty of Medical Sciences, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
Pediatr Neurol ; 50(4): 368-76, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24630283
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Reação em Cadeia da Polimerase / Técnicas de Diagnóstico Molecular / Síndrome do Cromossomo X Frágil / Deficiência Intelectual / Metilação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Reação em Cadeia da Polimerase / Técnicas de Diagnóstico Molecular / Síndrome do Cromossomo X Frágil / Deficiência Intelectual / Metilação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2014 Tipo de documento: Article