• A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters' anomaly
• A case of Peters' anomaly in a springer spaniel
• A Case of WAGR Syndrome with Peters' Anomaly
• A donor twin discordant with Peters anomaly in a twin-twin transfusion syndrome case: a case report
• A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrum
• A novel histopathologic finding in the Descemet's membrane of a patient with Peters Anomaly: a case-report and literature review
• A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomaly
• A novel phenotype associated with the R162W variant in the <em>KCNJ13</em> gene
• A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly
• A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report
• Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015
• Adams-Oliver syndrome: a case of bilateral progressive ischemic maculopathy
• Analysis of FOXD3 sequence variation in human ocular disease
• Anterior segment dysgenesis (Peters' anomaly) in two snow leopard (Panthera uncia) cubs
• Anterior segment dysgenesis correlation with epithelial-mesenchymal transition in Smad4 knockout mice
• Anterior segment mesenchymal dysgenesis in a large Australian family is associated with the recurrent 17 bp duplication in PITX3
• Approach to childhood glaucoma: A review
• Autosomal dominant cataracts and Peters anomaly in a large Australian family
• Bilateral diffuse iris nodular nevi. Clinical and histopathologic characterization
• Bilateral primary hyperplastic persistent vitreous: report of two cases
• Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous
• Case report of the rare Peters' anomaly complicated with Axenfeld-Rieger syndrome: A case report and brief review of the literature
• Cataract formation in Peter's anomaly after trabeculotomy
• Cataract surgery for tilted lens in peters' anomaly type 2
• Cataract surgery in children with congenital keratolenticular adhesion (Peters anomaly type 2)
• Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma
• Clinical effects of pediatric penetrating keratoplasty for congenital corneal opacity
• Clinical Outcomes Of Descemet Membrane Endothelial Keratoplasty Using The Bonfadini-Todd Injector For Graft Insertion
• Clinicopathologic Features and Treatment Characteristics of Congenital Corneal Opacity Infants and Children Aged 3 Years or Less: A Retrospective Single Institution Analysis
• Combined vitrectomy and glaucoma drainage device implantation surgical approach for complex pediatric glaucomas
• Deficiency of the RNA binding protein caprin2 causes lens defects and features of Peters anomaly
• Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1
• First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
• First Report of Mexican Patients with <em>PACS1</em>-Related Neurodevelopmental Disorder and Review of the <em>PACS1</em>-, <em>PACS2</em>-, and <em>WDR37</em>-Related Ophthalmological Manifestations
• Forme fruste anterior segment dysgenesis
• FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1
• Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
• Genetic dissection of anterior segment dysgenesis caused by a <em>Col4a1</em> mutation in mouse
• Glaucoma Surgery in Anterior Segment Dysgeneses
• Harboyan Syndrome
• Histopathological examination of two cases of anterior staphyloma associated with Peters' anomaly and persistent hyperplastic primary vitreous
• Identification of a New Genetic Mutation Associated With Peters Anomaly
• Identification of PITX3 mutations in individuals with various ocular developmental defects
• Image-guided femtosecond laser-assisted cataract surgery in Peters anomaly type 2
• Intensive intracorneal keloid formation in a case of Peters plus syndrome and in Peters anomaly with maximum manifestation
• Interstitial deletion 2q14q21
• Keratolenticular adhesion removal for type 2 Peters anomaly: a case report
• Long-term results of corneal graft survival in infants and children with peters anomaly
• Long-term visual outcome of penetrating keratoplasty in infants and children with Peters anomaly
• Long-Term Visual Outcomes and Clinical Course of Patients With Peters Anomaly
• Long-term visual prognosis in children after corneal transplant surgery for Peters anomaly type I
• Megalocornea
• Missense mutation at the C-terminus of PAX6 negatively modulates homeodomain function
• Missense mutation in the alternative splice region of the PAX6 gene in eye anomalies
• Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGFbeta2 in the pathogenesis of Peters' anomaly
• Mooren's ulcer and evidence of stromal graft rejection after penetrating keratoplasty
• Mutations of the PAX6 gene detected in patients with a variety of optic-nerve malformations
• Newborn with bilateral hazy corneas
• Novel heterozygous variants in <em>PXDN</em> cause different anterior segment dysgenesis phenotypes in monozygotic twins
• Ocular findings in a 4 p- deletion syndrome (Wolf-Hirschhorn)
• Ocular manifestations in Peters' syndrome
• Oculocerebral hypopigmentation syndrome (Cross syndrome) in a Gipsy child
• Ophthalmological assessment of crizotinib in advanced non-small-cell lung cancer
• Optical iridectomy for corneal opacities in Peter's anomaly
• Optimising keratoplasty for Peters' anomaly in infants using spectral-domain optical coherence tomography
• PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?
• PAX6 mutations reviewed
• PAX8 Expression in the Crystalline Lens and Lens-Derived Lesions
• Persistent hyperplastic primary vitreous with myopia: a case study
• Peters Anomaly
• Peters anomaly in association with multiple midline anomalies and a familial chromosome 4 inversion
• Peters Anomaly in Twins: A Case Report of a Rare Incident with Novel Comorbidities
• Peters Plus Syndrome
• Peters' anomaly and combination with other malformations (series of 16 patients)
• Peters' anomaly: a clinicopathologic study
• Peters' anomaly. A synopsis of surgical management and visual outcome
• POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome
• Posterior lamellar keratoplasty (DSAEK) in Peters anomaly
• Prenatal detection of Peters plus-like syndrome
• Prognostic factors of pediatric glaucoma: a retrospective study
• RNA-binding proteins in eye development and disease: implication of conserved RNA granule components
• Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies
• Should unilateral congenital corneal opacities in Peters' anomaly be grafted?
• Surgical approach in type II Peters anomaly - case report
• Surgical management of glaucoma in infants and children with Peters' anomaly: long-term structural and functional outcome
• Systemic Associations of Childhood Glaucoma: A Review
• The role of the abnormalities in the distal pathway of cholesterol biosynthesis in the Conradi-Hünermann-Happle syndrome
• Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities
• Thromboembolism and congenital malformations: from Duane syndrome to thalidomide embryopathy
• Transplantation of congenitally opaque corneas
• Type II Peter's anomaly with histopathological proof: a case report
• Ultrastructure of anterior lens capsule in Peters' plus syndrome
• Unilateral buphthalmos, corneal staphyloma and corneal fistula caused by pathogenic variant in the PITX3 gene: a case report
• Unilateral Peters' anomaly complicated by a corneal tattoo
• Unilateral Peters' anomaly with chorioretinal coloboma in the other eye
• Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
• Visual impairment and ocular abnormalities in children with fetal alcohol syndrome
• Visual outcome after surgery for Peters' anomaly
• Vitreoretinal dysplasia masquerading as Peters' anomaly
• Zebrafish pitx3 is necessary for normal lens and retinal development