Anterior Segment Dysgenesis
Last Posted: Dec 19, 2019
- Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Lenassi Eva et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Dec
- Genetic Testing in Pediatric Ophthalmology.
Verma Ishwar Chander et al. Indian journal of pediatrics 2017 Oct
- Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.
Reis Linda M, et al. Molecular vision 2016 0 1229-1238
- Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma.
Huang Xiaobo, et al. International journal of molecular medicine 2015 10 (4) 1111-7
- Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations.
D'haene Barbara, et al. Investigative ophthalmology & visual science 2011 1 (1) 324-33
- FOXE3 plays a significant role in autosomal recessive microphthalmia.
Reis Linda M, et al. American journal of medical genetics. Part A 2010 3 (3) 582-90
- The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.
Chakrabarti Subhabrata, et al. Investigative ophthalmology & visual science 2009 1 (1) 75-83
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