• <em>ADAMTSL4-</em>Related Eye Disorders
• A novel ADAMTSL4 compound heterozygous mutation in isolated ectopia lentis: a case report and review of the literature
• A novel mutation in the aspartate beta-hydroxylase (<em>ASPH</em>) gene is associated with a rare form of Traboulsi syndrome
• A rare presentation of bilateral dislocated lens in a patient with isolated microspherophakia
• ADAMTSL4-associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype description
• ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent
• Clinical and genetic findings in Chinese families with congenital ectopia lentis
• Early onset ectopia lentis due to a FBN1 mutation with non-penetrance
• Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families
• Familial Ectopia Lentis: Looking Beyond Marfan's Syndrome
• Genotype variant screening and phenotypic analysis of <em>FBN1</em> in Chinese patients with isolated ectopia lentis
• Hereditary ectopia lentis
• How far is observation allowed in patients with ectopia lentis?
• Isolated sulfite oxidase deficiency: a founder mutation
• Mutation analysis of SUOX in isolated sulfite oxidase deficiency with ectopia lentis as the presenting feature: insights into genotype-phenotype correlation
• Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis
• Novel <em>ADAMTSL4</em> gene mutations in Chinese patients with isolated ectopia lentis
• Novel compound heterozygous mutations identified in ADAMTSL4 gene in a Chinese family with isolated ectopia lentis
• Novel p.G1344E mutation in <em>FBN1</em> is associated with ectopia lentis
• Ophthalmic findings in a family with early-onset isolated ectopia lentis and the p.Arg62Cys mutation of the fibrillin-1 gene (FBN1)
• Portable femtosecond laser assisted cataract surgery in a child with bilateral ectopia lentis with microspherophakia
• Recurrent Intraocular Lens Dislocation in a Patient with Familial Ectopia Lentis
• Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: sibling case report and literature review
• Surgical management of non-syndromic ectopia lentis
• The revised ghent nosology; reclassifying isolated ectopia lentis
• The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis
• Zonule-Associated Gene Variants in Isolated Ectopia Lentis and Glaucoma