Your browser doesn't support javascript.
loading
Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy.
Shurygina, Maria F; Simonett, Joseph M; Parker, Maria A; Mitchell, Amanda; Grigorian, Florin; Lifton, Jacob; Nagiel, Aaron; Shpak, Alexander A; Dadali, Elena L; Mishina, Irina A; Weleber, Richard G; Yang, Paul; Pennesi, Mark E.
Afiliação
  • Shurygina MF; S. Fyodorov Eye Microsurgery Federal State Institution, Moscow, Russia.
  • Simonett JM; Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, United States.
  • Parker MA; Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, United States.
  • Mitchell A; Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, United States.
  • Grigorian F; University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States.
  • Lifton J; Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, California, United States.
  • Nagiel A; Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, California, United States.
  • Shpak AA; The Vision Center, Department of Surgery, Children's Hospital Los Angeles, Los Angeles, California, United States.
  • Dadali EL; The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, United States.
  • Mishina IA; S. Fyodorov Eye Microsurgery Federal State Institution, Moscow, Russia.
  • Weleber RG; The Vision Center, Department of Surgery, Children's Hospital Los Angeles, Los Angeles, California, United States.
  • Yang P; The Vision Center, Department of Surgery, Children's Hospital Los Angeles, Los Angeles, California, United States.
  • Pennesi ME; Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, United States.
Invest Ophthalmol Vis Sci ; 61(13): 2, 2020 11 02.
Article em En | MEDLINE | ID: mdl-33137195
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Cinesinas / Vitreorretinopatias Exsudativas Familiares / Microcefalia / Proteínas Associadas aos Microtúbulos / Mutação Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Invest Ophthalmol Vis Sci Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Retinianas / Cinesinas / Vitreorretinopatias Exsudativas Familiares / Microcefalia / Proteínas Associadas aos Microtúbulos / Mutação Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Invest Ophthalmol Vis Sci Ano de publicação: 2020 Tipo de documento: Article