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Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies.
Azab, Bilal; Dardas, Zain; Aburizeg, Dunia; Al-Bdour, Muawyah; Abu-Ameerh, Mohammed; Saleh, Tareq; Barham, Raghda; Maswadi, Ranad; Ababneh, Nidaa A; Alsalem, Mohammad; Zouk, Hana; Amr, Sami; Awidi, Abdalla.
Afiliação
  • Azab B; Department of Human and Molecular Genetics, School of Medicine, Virginia Commonwealth University, Richmond, VA 23298-0565, USA.
  • Dardas Z; Department of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.
  • Aburizeg D; Department of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.
  • Al-Bdour M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
  • Abu-Ameerh M; Department of Pathology and Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan.
  • Saleh T; Department of Ophthalmology, Jordan University Hospital, The University of Jordan, Amman 11942, Jordan.
  • Barham R; Department of Ophthalmology, Jordan University Hospital, The University of Jordan, Amman 11942, Jordan.
  • Maswadi R; Department of Basic Medical Sciences, Faculty of Medicine, The Hashemite University, Zarqa 13115, Jordan.
  • Ababneh NA; Cell Therapy Center, The University of Jordan, Amman 11942, Jordan.
  • Alsalem M; Department of Ophthalmology, Guy's and St Thomas' NHS Foundation Trust, London SE1 7EH, UK.
  • Zouk H; Cell Therapy Center, The University of Jordan, Amman 11942, Jordan.
  • Amr S; Department of Anatomy and Histology, School of Medicine, The University of Jordan, Amman 11942, Jordan.
  • Awidi A; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, MA 02139, USA.
Genes (Basel) ; 12(4)2021 04 19.
Article em En | MEDLINE | ID: mdl-33921607
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Marcadores Genéticos / Predisposição Genética para Doença / Distrofias Retinianas / Exoma / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Marcadores Genéticos / Predisposição Genética para Doença / Distrofias Retinianas / Exoma / Mutação Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos