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The morbid genome of ciliopathies: an update.
Shamseldin, Hanan E; Shaheen, Ranad; Ewida, Nour; Bubshait, Dalal K; Alkuraya, Hisham; Almardawi, Elham; Howaidi, Ali; Sabr, Yasser; Abdalla, Ebtesam M; Alfaifi, Abdullah Y; Alghamdi, Jameel Mohammed; Alsagheir, Afaf; Alfares, Ahmed; Morsy, Heba; Hussein, Maged H; Al-Muhaizea, Mohammad A; Shagrani, Mohammad; Al Sabban, Essam; Salih, Mustafa A; Meriki, Neama; Khan, Rubina; Almugbel, Maisoon; Qari, Alya; Tulba, Maha; Mahnashi, Mohammed; Alhazmi, Khalid; Alsalamah, Abrar K; Nowilaty, Sawsan R; Alhashem, Amal; Hashem, Mais; Abdulwahab, Firdous; Ibrahim, Niema; Alshidi, Tarfa; AlObeid, Eman; Alenazi, Mona M; Alzaidan, Hamad; Rahbeeni, Zuhair; Al-Owain, Mohammed; Sogaty, Sameera; Seidahmed, Mohammed Zain; Alkuraya, Fowzan S.
Affiliation
  • Shamseldin HE; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Shaheen R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Ewida N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Bubshait DK; Department of Pediatrics, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
  • Alkuraya H; Department of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
  • Almardawi E; Department of Obstetrics and Gynecology, Security Forces Hospital, Riyadh, Saudi Arabia.
  • Howaidi A; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Sabr Y; Deparment of Obstetrics and Gynecology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Abdalla EM; Human Genetics Department, Medical Research Institute, Alexandria University, Alexandria, Egypt.
  • Alfaifi AY; Department of Pediatrics, Security Forces Hospital, Riyadh, Saudi Arabia.
  • Alghamdi JM; Department of Pediatrics, College of Medicine, AlBaha University, AlBaha, Saudi Arabia.
  • Alsagheir A; Endocrinology Section, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alfares A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Morsy H; Human Genetics Department, Medical Research Institute, Alexandria University, Alexandria, Egypt.
  • Hussein MH; Nephrology Section, Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Muhaizea MA; Department of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Shagrani M; Organ Transplant Center, King Faisal Specialist Hospital and Research Center, and College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Al Sabban E; Nephrology Section, Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Salih MA; Division of Pediatric Neurology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Meriki N; Department of Obstetrics and Gynecology, Security Forces Hospital, Riyadh, Saudi Arabia.
  • Khan R; Depatment of Obstetrics and Gynecology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Almugbel M; Depatment of Obstetrics and Gynecology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Qari A; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Tulba M; Depatment of Obstetrics and Gynecology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Mahnashi M; Divison of Genetics, Department of General Pediatrics, King Fahad Central Hospital, Jazan, Saudi Arabia.
  • Alhazmi K; Divison of Genetics, Department of General Pediatrics, King Fahad Central Hospital, Jazan, Saudi Arabia.
  • Alsalamah AK; Vitreoretinal Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
  • Nowilaty SR; Vitreoretinal Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
  • Alhashem A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Hashem M; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alshidi T; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • AlObeid E; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alenazi MM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alzaidan H; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Rahbeeni Z; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Owain M; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Sogaty S; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Seidahmed MZ; Department of Pediatrics, King Fahad General Hospital, Jeddah, Saudi Arabia.
  • Alkuraya FS; Department of Pediatrics, Security Forces Hospital, Riyadh, Saudi Arabia.
Genet Med ; 22(6): 1051-1060, 2020 06.
Article in En | MEDLINE | ID: mdl-32055034
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Full text: 1 Database: MEDLINE Main subject: Bardet-Biedl Syndrome / Ciliopathies Limits: Humans Language: En Year: 2020 Type: Article
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Bardet-Biedl Syndrome / Ciliopathies Limits: Humans Language: En Year: 2020 Type: Article