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Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel.
Al-Hamed, Mohamed H; Kurdi, Wesam; Alsahan, Nada; Alabdullah, Zainab; Abudraz, Rania; Tulbah, Maha; Alnemer, Maha; Khan, Rubina; Al-Jurayb, Haya; Alahmed, Ahmed; Tahir, Asma I; Khalil, Dania; Edwards, Noel; Al Abdulaziz, Basma; Binhumaid, Faisal S; Majid, Salma; Faquih, Tariq; El-Kalioby, Mohamed; Abouelhoda, Mohamed; Altassan, Nada; Monies, Dorota; Meyer, Brian; Sayer, John A; Albaqumi, Mamdouh.
Afiliación
  • Al-Hamed MH; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Kurdi W; Obstetrics and Gynecology Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Alsahan N; Obstetrics and Gynecology Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Alabdullah Z; Obstetrics & Gynecology Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Abudraz R; Obstetrics and Gynecology Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Tulbah M; Obstetrics and Gynecology Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Alnemer M; Obstetrics and Gynecology Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Khan R; Obstetrics and Gynecology Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Al-Jurayb H; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Alahmed A; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Tahir AI; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Khalil D; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Edwards N; Institute of Genetic Medicine, International Centre for Life, Newcastle University, Newcastle upon Tyne, UK.
  • Al Abdulaziz B; Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Binhumaid FS; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Majid S; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Faquih T; Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • El-Kalioby M; Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Abouelhoda M; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Altassan N; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Monies D; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Meyer B; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Saudi Human Genome Project, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Sayer JA; Institute of Genetic Medicine, International Centre for Life, Newcastle University, Newcastle upon Tyne, UK.
  • Albaqumi M; Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia Medicine Department, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
J Med Genet ; 53(5): 338-47, 2016 05.
Article en En | MEDLINE | ID: mdl-26862157
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Análisis Mutacional de ADN / Enfermedades Renales Quísticas / Feto / Ciliopatías / Mutación Tipo de estudio: Prognostic_studies Límite: Female / Humans / Newborn / Pregnancy País/Región como asunto: Asia Idioma: En Revista: J Med Genet Año: 2016 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Análisis Mutacional de ADN / Enfermedades Renales Quísticas / Feto / Ciliopatías / Mutación Tipo de estudio: Prognostic_studies Límite: Female / Humans / Newborn / Pregnancy País/Región como asunto: Asia Idioma: En Revista: J Med Genet Año: 2016 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Reino Unido