• ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome
• Clinical utility gene card for: Peters plus syndrome
• Contribution of a Novel <em>B3GLCT</em> Variant to Peters Plus Syndrome Discovered by a Combination of Next-Generation Sequencing and Automated Text Mining
• Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome
• High-Throughput miRFluR Platform Identifies miRNA Regulating B3GLCT That Predict Peters' Plus Syndrome Phenotype, Supporting the miRNA Proxy Hypothesis
• Mobile Retrolental Cyst in a Child With Peters Plus Syndrome
• Ocular Phenotype of Peters-Plus Syndrome
• Peters Anomaly
• Peters Anomaly
• PETERS ANOMALY AND PETERS PLUS SYNDROME
• Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report
• Peters plus syndrome mutations affect the function and stability of human β1,3-glucosyltransferase
• Peters Plus syndrome: a recognizable clinical entity
• Peters-plus syndrome: Report of a rare case
• Prenatal Detection of Peters' Plus Syndrome in a Patient with No Known Family History
• Unique Presentation of Corneal Opacity in Peters Plus Syndrome: An Unusual Form of Peters Anomaly Showing Tissue Repair in Serial Analysis
• Whole-exome sequencing for diagnosis of Peters-plus syndrome after prenatal diagnosis of recurrent low PAPP-A and multiple fetal anomalies in two consecutive pregnancies