• <em>ADAMTS18</em>-related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome
• 4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental Delay
• A patient with concurrent Axenfeld-Rieger and Stickler syndromes verified by molecular genetics
• ADAMTS18-related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome
• Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum
• Axenfeld anomaly with persistent pupillary membrane
• Axenfeld-Reiger syndrome: A search for the missing links
• Axenfeld-Rieger anomaly with slit pupils
• Axenfeld-Rieger Syndrome
• Axenfeld-Rieger Syndrome and Possible Airway Complications
• Axenfeld-Rieger syndrome combined with ectropion uveae and pigment dispersion syndrome: A case report
• Axenfeld-Rieger syndrome in the pediatric population: A review
• Axenfeld-Rieger syndrome: a novel histopathologic finding associated with corneal abnormalities
• Axenfeld-Rieger syndrome: A systematic review examining genetic, neurological, and neurovascular associations to inform screening
• Case Report: Congenital Pseudoacorea in an Ocular Axenfeld-Rieger Syndrome: What is it?
• Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome
• Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features
• Clinical and Genetic Correlation in Neurocristopathies: Bridging a Precision Medicine Gap
• Commercial Gene Panels for Congenital Anterior Segment Anomalies: Are They All the Same?
• Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome
• Craniofacial and dental features of Axenfeld-Rieger syndrome patients with PITX2 mutations
• Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease
• Glaucoma drainage device implantation in a pregnant woman with axenfeld-rieger syndrome
• In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene
• In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome
• Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2
• Intragenic FOXC1 deletion in a Vietnamese child with Axenfeld-Rieger syndrome: case report and review of literature
• Leukoencephalopathy with spot-like calcifications caused by recessive COL4A2 variants
• Megalocornea
• Microspherophakia
• Microspherophakia: A clinical approach and mini review with a case report
• Modified horizontal muscle transposition without tenotomy and splitting for a case of inferior rectus and inferior oblique muscles aplasia with hemifacial microsomia
• Neuroimaging Findings in Axenfeld-Rieger Syndrome: A Case Series
• Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review
• Ophthalmological Manifestations of Axenfeld-Rieger Syndrome: Current Perspectives
• Penetrating Keratoplasty in Congenital Glaucoma
• Posterior embryotoxon as the initial ophthalmological sign of Axenfeld-Rieger syndrome
• Primary Cilium in Neural Crest Cells Crucial for Anterior Segment Development and Corneal Avascularity
• The clinical and genetic findings in a Chinese family with Axenfeld-Rieger syndrome
• The morphology of angle dysgenesis assessed by ultrasound biomicroscopy and its relationship with glaucoma severity and mutant genes in Axenfeld-Rieger syndrome
• UNC-30/PITX coordinates neurotransmitter identity with postsynaptic GABA receptor clustering
• Whole genome sequencing in families with oligodontia