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Common disease-associated gene variants in a Saudi Arabian population.
Aleissa, Mariam; Aloraini, Taghrid; Alsubaie, Lamia Fahad; Hassoun, Madawi; Abdulrahman, Ghada; Swaid, Abdulrahman; Eyaid, Wafa Al; Mutairi, Fuad Al; Ababneh, Faroug; Alfadhel, Majid; Alfares, Ahmed.
Afiliación
  • Aleissa M; From the Division of Translational Pathology, Department of Laboratory Medicine, King Abdulaziz Medical City.
  • Aloraini T; From the Department of Molecular Genetics, Public Health Laboratory, Public Health Authority, Riyadh.
  • Alsubaie LF; From the College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Hassoun M; From the Division of Translational Pathology, Department of Laboratory Medicine, King Abdulaziz Medical City.
  • Abdulrahman G; From the King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences.
  • Swaid A; From the Department of Genetics, King Abdullah Specialized Children Hospital, King Abdulaziz Medical City, MNGHA.
  • Eyaid WA; From the King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences.
  • Mutairi FA; From the Division of Translational Pathology, Department of Laboratory Medicine, King Abdulaziz Medical City.
  • Ababneh F; From the King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences.
  • Alfadhel M; From the Division of Translational Pathology, Department of Laboratory Medicine, King Abdulaziz Medical City.
  • Alfares A; From the King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences.
Ann Saudi Med ; 42(1): 29-35, 2022.
Article en En | MEDLINE | ID: mdl-35112591

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Familia / Genética de Población / Enfermedades Genéticas Congénitas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Ann Saudi Med Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article Pais de publicación:

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Familia / Genética de Población / Enfermedades Genéticas Congénitas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Ann Saudi Med Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article Pais de publicación: