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Absence of Goniodysgenesis in Patients with Chromosome 13Q Microdeletion-Related Microcoria.
Gerth-Kahlert, Christina; Maggi, Jordi; Töteberg-Harms, Marc; Tiwari, Amit; Budde, Birgit; Nürnberg, Peter; Koller, Samuel; Berger, Wolfgang.
Afiliação
  • Gerth-Kahlert C; Department of Ophthalmology, University Hospital Zurich, Zurich, Switzerland. Electronic address: christina.gerth-kahlert@usz.ch.
  • Maggi J; Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland.
  • Töteberg-Harms M; Department of Ophthalmology, University Hospital Zurich, Zurich, Switzerland.
  • Tiwari A; Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland.
  • Budde B; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Nürnberg P; Cologne Center for Genomics, University of Cologne, Cologne, Germany; Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, Cologne, Germany.
  • Koller S; Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland.
  • Berger W; Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland; Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland; Neuroscience Center Zurich, University and ETH Zurich, Zurich, Switzerland.
Ophthalmol Glaucoma ; 1(2): 145-147, 2018.
Article em En | MEDLINE | ID: mdl-32672565
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 13 / Anormalidades do Olho / Câmara Anterior Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ophthalmol Glaucoma Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 13 / Anormalidades do Olho / Câmara Anterior Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ophthalmol Glaucoma Ano de publicação: 2018 Tipo de documento: Article