Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference12 articles.
1. Submicroscopic deletions at 13q32.1 cause congenital microcoria;Fares-Taie;Am. J. Hum. Genet.,2015
2. Congenital miosis or pinhole pupils owing to developmental faults of the dilatator muscle;Holth;Br. J. Ophthalmol.,1923
3. An unusual congenital and familial congenital malformative combination involving the eye and kidney;Pierson;J. Genet. Hum.,1963
4. Ultrabiomicroscopic-histopathologic correlations in individuals with autosomal dominant congenital microcoria: three-generation family report;Ramirez-Miranda;Case Rep Ophthalmol,2011
5. Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma;Sergouniotis;Acta Ophthalmol.,2017
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