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Characterizing the morbid genome of ciliopathies.
Shaheen, Ranad; Szymanska, Katarzyna; Basu, Basudha; Patel, Nisha; Ewida, Nour; Faqeih, Eissa; Al Hashem, Amal; Derar, Nada; Alsharif, Hadeel; Aldahmesh, Mohammed A; Alazami, Anas M; Hashem, Mais; Ibrahim, Niema; Abdulwahab, Firdous M; Sonbul, Rawda; Alkuraya, Hisham; Alnemer, Maha; Al Tala, Saeed; Al-Husain, Muneera; Morsy, Heba; Seidahmed, Mohammed Zain; Meriki, Neama; Al-Owain, Mohammed; AlShahwan, Saad; Tabarki, Brahim; Salih, Mustafa A; Faquih, Tariq; El-Kalioby, Mohamed; Ueffing, Marius; Boldt, Karsten; Logan, Clare V; Parry, David A; Al Tassan, Nada; Monies, Dorota; Megarbane, Andre; Abouelhoda, Mohamed; Halees, Anason; Johnson, Colin A; Alkuraya, Fowzan S.
Afiliação
  • Shaheen R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Szymanska K; Leeds Institute of Biomedical & Clinical Sciences, University of Leeds, Leeds, LS9 7TF, UK.
  • Basu B; Leeds Institute of Biomedical & Clinical Sciences, University of Leeds, Leeds, LS9 7TF, UK.
  • Patel N; 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.
  • Faqeih E; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Al Hashem A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Derar N; Department of Pediatrics, Division of Medical Genetics, Stanford University, Stanford, CA, USA.
  • Alsharif H; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Aldahmesh MA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alazami AM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Hashem M; 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.
  • Abdulwahab FM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Sonbul R; Department of Pediatrics, Qatif Central Hospital, Qatif, Saudi Arabia.
  • Alkuraya H; Department of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
  • Alnemer M; Department of Obstetrics and Gynecology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al Tala S; Department of Pediatric, Genetic Unit, Armed Forces Hospital Southern Region, Khamis Mushayt, Saudi Arabia.
  • Al-Husain M; Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Morsy H; Human Genetics Department, Medical Research Institute, Alexandria University, Alexandria, Egypt.
  • Seidahmed MZ; Department of Pediatrics, Security Forces Hospital, Riyadh, Saudi Arabia.
  • Meriki N; Department of Obstetrics and Gynecology, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Al-Owain M; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • AlShahwan S; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Tabarki B; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Salih MA; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • El-Kalioby M; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Ueffing M; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Boldt K; Division of Experimental Ophthalmology and Medical Bioanalytics, Center for Ophthalmology, Eberhard-Karls University Tübingen, 72076, Tübingen, Germany.
  • Logan CV; Division of Experimental Ophthalmology and Medical Bioanalytics, Center for Ophthalmology, Eberhard-Karls University Tübingen, 72076, Tübingen, Germany.
  • Parry DA; Leeds Institute of Biomedical & Clinical Sciences, University of Leeds, Leeds, LS9 7TF, UK.
  • Al Tassan N; Leeds Institute of Biomedical & Clinical Sciences, University of Leeds, Leeds, LS9 7TF, UK.
  • Monies D; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Megarbane A; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Abouelhoda M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Halees A; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Johnson CA; Institut Jerome Lejeune, Paris, France.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Genome Biol ; 17(1): 242, 2016 11 28.
Article em En | MEDLINE | ID: mdl-27894351

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cílios / Transtornos da Motilidade Ciliar / Encefalocele / Ciliopatias / Doenças Renais Policísticas / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Genome Biol Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Arábia Saudita País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cílios / Transtornos da Motilidade Ciliar / Encefalocele / Ciliopatias / Doenças Renais Policísticas / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Genome Biol Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Arábia Saudita País de publicação: Reino Unido