Your browser doesn't support javascript.
loading
Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene.
Ibarra-Ramírez, Marisol; Fernandez-de-Luna, Marissa L; Campos-Acevedo, Luis D; Arenas-Estala, Joel; Martínez-de-Villarreal, Laura E; Rodríguez-Garza, Claudia; DeLagarza-Pineda, Oscar; Mohamed-Noriega, Jibran.
Afiliação
  • Ibarra-Ramírez M; Department of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • Fernandez-de-Luna ML; Department of Ophthalmology, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • Campos-Acevedo LD; Department of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • Arenas-Estala J; Department of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • Martínez-de-Villarreal LE; Department of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • Rodríguez-Garza C; Department of Radiology and Imaging, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • DeLagarza-Pineda O; Department of Neurology, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
  • Mohamed-Noriega J; Department of Ophthalmology, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Mexico.
Ophthalmic Genet ; 44(5): 465-468, 2023 10.
Article em En | MEDLINE | ID: mdl-37519288
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrogripose / Estrabismo / Deficiência Intelectual / Microcefalia Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Revista: Ophthalmic Genet Assunto da revista: GENETICA MEDICA / OFTALMOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: México
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrogripose / Estrabismo / Deficiência Intelectual / Microcefalia Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans Idioma: En Revista: Ophthalmic Genet Assunto da revista: GENETICA MEDICA / OFTALMOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: México