Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes - ScienceDirect
What is Stickler syndrome? | Vinmec
Clinical and molecular genetics of Stickler syndrome | Journal of Medical Genetics
Genes | Free Full-Text | Hearing Loss in Stickler Syndrome: An Update
Overview of the four individuals with Marshall-Stickler syndrome | Download Table
A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype–phenotype correlations in type XI collagenopathies - Majava - 2007 - American Journal of Medical
JPM | Free Full-Text | Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation
A rare case of stickler marshall syndrome
Stickler syndrome
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix. - Abstract - Europe
Stickler syndrome: Clinical characteristics and diagnostic criteria - Rose - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library
Arthralgias and Articular Hyperlaxitude in Women with Ophthalmopathy and Early Deafness | Reumatología Clínica