The Role of Genetic Testing in Childhood Glaucoma
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-19-7466-3_3
Reference18 articles.
1. Alward WLM. Axenfeld-Rieger syndrome in the age of molecular genetics. Am J Opthalmol. 2000;130(1):107–15.
2. Bhatia S, Bengani H, Fish M, et al. Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia. Am J Hum Genet. 2013;93(6):1126–34.
3. Franzoni A, Russo PD, Baldan F, D'Elia AV, Puppin C, Penco S, Damante G. A CGH array procedure to detect PAX6 gene structural defects. Mol Cell Probes. 2017;32:65–8.
4. Gupta V, Markan A, Somarajan BI, Sihota R, Gupta A, Gupta S, Sharma A. Phenotypic differences between familial versus non-familial Juvenile onset open angle glaucoma patients. Ophthalmic Genet. 2018;39(1):63–7.
5. Khan AO. Genetics of primary glaucoma. Curr Opin Ophthalmol. 2011;22(5):347–55.
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