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Further delineation of Temtamy syndrome of corpus callosum and ocular abnormalities.
Alrakaf, Laila; Al-Owain, Mohammed A; Busehail, Maryam; Alotaibi, Maha A; Monies, Dorota; Aldhalaan, Hesham M; Alhashem, Amal; Al-Hassnan, Zuhair N; Rahbeeni, Zuhair A; Murshedi, Fathiya Al; Ani, Nadia Al; Al-Maawali, Almundher; Ibrahim, Niema A; Abdulwahab, Firdous M; Alsagob, Maysoon; Hashem, Mais O; Ramadan, Wafaa; Abouelhoda, Mohamed; Meyer, Brian F; Kaya, Namik; Maddirevula, Sateesh; Alkuraya, Fowzan S.
Afiliação
  • Alrakaf L; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Al-Owain MA; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Busehail M; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Alotaibi MA; Clinical Genetic and Metabolic Department, King Saud Medical city, Riyadh, Saudi Arabia.
  • Monies D; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Aldhalaan HM; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
  • Alhashem A; Department of Neuroscience, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Hassnan ZN; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Rahbeeni ZA; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Murshedi FA; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Ani NA; Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Al-Maawali A; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Ibrahim NA; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Abdulwahab FM; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Alsagob M; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
  • Hashem MO; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
  • Ramadan W; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Abouelhoda M; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Meyer BF; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Kaya N; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Maddirevula S; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
  • Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital Research Center, Riyadh, Saudi Arabia.
Am J Med Genet A ; 176(3): 715-721, 2018 03.
Article em En | MEDLINE | ID: mdl-29383837
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coloboma / Anormalidades do Olho / Anormalidades Craniofaciais / Agenesia do Corpo Caloso Tipo de estudo: Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 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: Coloboma / Anormalidades do Olho / Anormalidades Craniofaciais / Agenesia do Corpo Caloso Tipo de estudo: Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Arábia Saudita