• "Eye of the hurricane" anterior polar cataract
• A familial anterior corneal degeneration: clinical aspects, histopathology and differential diagnosis
• A family of fuchs endothelial corneal dystrophy and anterior polar cataract with an analysis of whole exome sequencing
• A locus for autosomal dominant anterior polar cataract on chromosome 17p
• A novel human CRYGD mutation in a juvenile autosomal dominant cataract
• Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8
• Acquired anterior pyramidal cataract: A surgical misadventure
• Anterior polar cataract due to bee sting
• Anterior polar cataract: clinical spectrum and genetic linkage in a single family
• Anterior Polar Cataracts in a Newborn
• Anterior polar pyramidal cataract
• Anterior segment mesenchymal dysgenesis in a large Australian family is associated with the recurrent 17 bp duplication in PITX3
• Arrhythmogenic right ventricular dysplasia and anterior polar cataract
• Autosomal dominant anterior polar cataracts associated with a familial 2;14 translocation
• C.57 C > T Mutation in MIR 184 is Responsible for Congenital Cataracts and Corneal Abnormalities in a Five-generation Family from Galicia, Spain
• Cataracts in Havanese: genome wide association study reveals two loci associated with posterior polar cataract
• Clinical and genetic heterogeneity in autosomal dominant cataract
• Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA)
• Clinicopathological correlation between fibrous metaplasia of lens and anterior pyramidal cataract: a proposed etiology
• Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
• Congenital anterior polar cataract: a review of 63 cases
• Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea
• Expression map of human chromosome region 17p13.3, spanning the RP13 dominant retinitis pigmentosa locus, the Miller-Dieker lissencephaly syndrome (MDLS) region, and a putative tumour suppressor locus
• Familial congenital cornea guttata with anterior polar cataracts
• Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes
• Gene mapping and mutation detection in a family with congenital anterior polar cataract
• Gross remnants of the pupillary membrane, anterior polar cataract and microcornea in a mother and her children
• Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalities
• Investigating the Clinical Characteristics and <em>PITX3</em>Mutations of a Large Chinese Family with Anterior Segment Mesenchymal Dysgenesis and Congenital Posterior Polar Cataract
• LEFT ANTERIOR POLAR CATARACT IN A MOTHER AND DAUGHTER
• Microphthalmia-congenital anterior polar cataract. An autosomal dominant syndrome
• Mutation altering the miR-184 seed region causes familial keratoconus with cataract
• Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity
• Ophthalmologic features of Vici syndrome
• PAX6 aniridia and interhemispheric brain anomalies
• Pediatric Anterior Pyramidal Polar Cataract
• Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene
• Posterior polar cataract: genetic analysis of a large family
• Prevalence of and risk factors for age-related and anterior polar cataracts in a Korean population
• Prevalence of anterior polar cataracts in children and risk factors for amblyopia
• The histological absence of IgG4 positive plasma cells in juvenile xanthogranuloma; comments on 'Systemic juvenile xanthogranuloma: a case report and brief review'
• The mouse Cat4 locus maps to chromosome 8 and mutants express lens-corneal adhesion
• Transforming growth factor-beta1 represses E-cadherin production via slug expression in lens epithelial cells
• Unique advantage of gonioscopy for viewing an anterior pyramidal cataract
• Variable expressivity of autosomal dominant microcornea with cataract