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Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits.
Al-Nabhani, Maryam; Al-Rashdi, Samiya; Al-Murshedi, Fathiya; Al-Kindi, Adila; Al-Thihli, Khalid; Al-Saegh, Abeer; Al-Futaisi, Amna; Al-Mamari, Watfa; Zadjali, Fahad; Al-Maawali, Almundher.
Afiliación
  • Al-Nabhani M; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Al-Rashdi S; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Al-Murshedi F; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Al-Kindi A; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Thihli K; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Al-Saegh A; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Al-Futaisi A; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Al-Mamari W; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Zadjali F; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Al-Maawali A; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
Clin Genet ; 94(6): 495-501, 2018 12.
Article en En | MEDLINE | ID: mdl-30125339
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Exoma / Secuenciación del Exoma / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Año: 2018 Tipo del documento: Article País de afiliación: Omán
Texto completo
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XML
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Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Exoma / Secuenciación del Exoma / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Año: 2018 Tipo del documento: Article País de afiliación: Omán