• Association of <em>EFEMP1</em> with juvenile-onset open angle glaucoma in a patient with concomitant <em>COL11A1</em>-related Stickler syndrome
• Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2)
• Case report: Autosomal recessive type 3 Stickler syndrome caused by compound heterozygous mutations in <em>COL11A2</em>
• Clinical Impact of Genetic Diagnosis of Sensorineural Hearing Loss in Adults
• Genetic testing in four Indian families with suspected Stickler syndrome
• Genetics of the pediatric glaucomas
• Incidence of mandibular distraction osteogenesis in Stickler Syndrome: Variation due to COL2A1 and COL11A1
• Laser Prophylaxis in Patients with Stickler Syndrome
• LEPREL1 -RELATED GIANT RETINAL TEAR DETACHMENTS MIMIC THE PHENOTYPE OF OCULAR STICKLER SYNDROME
• Long-term anatomical and functional outcomes of surgical treatment of retinal complications in children and adolescents with Stickler syndrome between 2004 and 2021
• Multidisciplinary approach to inherited causes of dual sensory impairment
• Premature arthritis is a distinct type II collagen phenotype: comment on the article by Kannu et al
• Progressive degeneration of the retina in Loxl3 mutant mouse model of Stickler syndrome
• Syndromes associated with Robin sequence: a national prospective cohort study
• The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia
• The Incidence of Velopharyngeal Insufficiency in Stickler Syndrome
• Window of Susceptibility to Acute Otitis Media Infection
• Zebrafish Model of Stickler Syndrome Suggests a Role for Col2a1a in the Neural Crest during Early Eye Development