Literature DB >> 32672565

Absence of Goniodysgenesis in Patients with Chromosome 13Q Microdeletion-Related Microcoria.

Christina Gerth-Kahlert1, Jordi Maggi2, Marc Töteberg-Harms3, Amit Tiwari2, Birgit Budde4, Peter Nürnberg5, Samuel Koller2, Wolfgang Berger6.   

Abstract

Entities:  

Year:  2018        PMID： 32672565     DOI： 10.1016/j.ogla.2018.08.003

Source DB:  PubMed          Journal:  Ophthalmol Glaucoma        ISSN： 2589-4196


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  2 in total

Review 1.  Congenital Microcoria: Clinical Features and Molecular Genetics.

Authors:  Clémentine Angée; Brigitte Nedelec; Elisa Erjavec; Jean-Michel Rozet; Lucas Fares Taie
Journal:  Genes (Basel)       Date:  2021-04-22       Impact factor: 4.096

2.  A rare case of congenital pupillary abnormality: a case report.

Authors:  Lancao Hao; Zicheng Ma; Chenjie Song; Siquan Zhu
Journal:  BMC Ophthalmol       Date:  2022-05-02       Impact factor: 2.209
  2 in total

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