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Genomic and phenotypic delineation of congenital microcephaly.
Shaheen, Ranad; Maddirevula, Sateesh; Ewida, Nour; Alsahli, Saud; Abdel-Salam, Ghada M H; Zaki, Maha S; Tala, Saeed Al; Alhashem, Amal; Softah, Ameen; Al-Owain, Mohammed; Alazami, Anas M; Abadel, Basma; Patel, Nisha; Al-Sheddi, Tarfa; Alomar, Rana; Alobeid, Eman; Ibrahim, Niema; Hashem, Mais; Abdulwahab, Firdous; Hamad, Muddathir; Tabarki, Brahim; Alwadei, Ali H; Alhazzani, Fahad; Bashiri, Fahad A; Kentab, Amal; Sahintürk, Serdar; Sherr, Elliott; Fregeau, Brieana; Sogati, Samira; Alshahwan, Saad Ali M; Alkhalifi, Salwa; Alhumaidi, Zainab; Temtamy, Samia; Aglan, Mona; Otaify, Ghada; Girisha, Katta M; Tulbah, Maha; Seidahmed, Mohammed Zain; Salih, Mustafa A; Abouelhoda, Mohamed; Momin, Afaque A; Saffar, Muna Al; Partlow, Jennifer N; Arold, Stefan T; Faqeih, Eissa; Walsh, Christopher; Alkuraya, Fowzan S.
Afiliación
  • Shaheen R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Maddirevula S; 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.
  • Alsahli S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Abdel-Salam GMH; Clinical Genetics Department, Human Genetics and Genome Research Division, Centre of Excellence of Human Genetics, National Research Centre, Cairo, Egypt.
  • Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Division, Centre of Excellence of Human Genetics, National Research Centre, Cairo, Egypt.
  • Tala SA; Department of Pediatrics, Genetic Unit, Armed Forces Hospital Southern Region, Khamis Mushayt, Saudi Arabia.
  • Alhashem A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Softah A; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Al-Owain M; King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
  • Alazami AM; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Abadel B; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Patel N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Sheddi T; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alomar R; 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.
  • Ibrahim N; 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.
  • Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Hamad M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Tabarki B; Division of Pediatric Neurology, College of Medicine and King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
  • Alwadei AH; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Alhazzani F; Pediatric Neurology Department, National Neuroscience Institute, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Bashiri FA; Pediatrics Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Kentab A; Division of Pediatric Neurology, College of Medicine and King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
  • Sahintürk S; Division of Pediatric Neurology, College of Medicine and King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
  • Sherr E; Faculty of Medicine, Physiology Department, Bursa Uludag University, Bursa, Turkey.
  • Fregeau B; Department of Neurology, University of California, San Francisco, California, USA.
  • Sogati S; Department of Neurology, University of California, San Francisco, California, USA.
  • Alshahwan SAM; Department of Medical Genetics, King Fahad General Hospital, Jeddah, Saudi Arabia.
  • Alkhalifi S; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Alhumaidi Z; Maternity and Children Hospital, Dammam, Saudi Arabia.
  • Temtamy S; Maternity and Children Hospital, Dammam, Saudi Arabia.
  • Aglan M; Clinical Genetics Department, Human Genetics and Genome Research Division, Centre of Excellence of Human Genetics, National Research Centre, Cairo, Egypt.
  • Otaify G; Clinical Genetics Department, Human Genetics and Genome Research Division, Centre of Excellence of Human Genetics, National Research Centre, Cairo, Egypt.
  • Girisha KM; Clinical Genetics Department, Human Genetics and Genome Research Division, Centre of Excellence of Human Genetics, National Research Centre, Cairo, Egypt.
  • Tulbah M; Department of Medical Genetics Kasturba Medical College, Manipal University (currently Manipal Academy of Higher Education), Manipal, India.
  • Seidahmed MZ; Department of obstetrics and gynecology king Faisal specialist hospital and research center, Riyadh, Saudi Arabia.
  • Salih MA; Department of Pediatrics, Security Forces Hospital, Riyadh, Saudi Arabia.
  • Abouelhoda M; Division of Pediatric Neurology, College of Medicine and King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.
  • Momin AA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Saffar MA; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Partlow JN; Computational Bioscience Research Center (CBRC), Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
  • Arold ST; Department of Paediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
  • Faqeih E; Division of Genetics and Genomics, Department of Medicine, Manton Center for Orphan Disease Research, Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Walsh C; Division of Genetics and Genomics, Department of Medicine, Manton Center for Orphan Disease Research, Howard Hughes Medical Institute, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Alkuraya FS; Computational Bioscience Research Center (CBRC), Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Genet Med ; 21(3): 545-552, 2019 03.
Article en En | MEDLINE | ID: mdl-30214071
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Microcefalia Límite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Año: 2019 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Microcefalia Límite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Año: 2019 Tipo del documento: Article