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Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
Al-Mubarak, Bashayer; Abouelhoda, Mohamed; Omar, Aisha; AlDhalaan, Hesham; Aldosari, Mohammed; Nester, Michael; Alshamrani, Hussain A; El-Kalioby, Mohamed; Goljan, Ewa; Albar, Renad; Subhani, Shazia; Tahir, Asma; Asfahani, Sultana; Eskandrani, Alaa; Almusaiab, Ahmed; Magrashi, Amna; Shinwari, Jameela; Monies, Dorota; Al Tassan, Nada.
Afiliação
  • Al-Mubarak B; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital & Research Center, P.O. Box 3354, Riyadh, 11211, Saudi Arabia. BAl-Mubarak@kfshrc.edu.sa.
  • Abouelhoda M; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia. BAl-Mubarak@kfshrc.edu.sa.
  • Omar A; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • AlDhalaan H; Department of Genetics, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Aldosari M; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital & Research Center, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Nester M; Center for Autism Research, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Alshamrani HA; Department of Neurosciences, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • El-Kalioby M; Center for Autism Research, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Goljan E; Department of Neurosciences, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Albar R; Pediatric Department, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Subhani S; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Tahir A; Department of Genetics, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Asfahani S; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Eskandrani A; Department of Genetics, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Almusaiab A; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Magrashi A; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Shinwari J; Department of Genetics, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Monies D; Behavioral Genetics unit, Department of Genetics, King Faisal Specialist Hospital & Research Center, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
  • Al Tassan N; Center for Autism Research, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
Sci Rep ; 7(1): 5679, 2017 07 18.
Article em En | MEDLINE | ID: mdl-28720891
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Espectro Autista / Sequenciamento do Exoma / Mutação Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Arábia Saudita
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Espectro Autista / Sequenciamento do Exoma / Mutação Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Arábia Saudita