The Stickler syndrome: Genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1 | Genetics in Medicine
Hereditary Vitreoretinal Degenerations | Ento Key
Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes - ScienceDirect
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
Stickler Syndrome: Symptoms & Outlook
Indian Pediatrics - Editorial
PDF] STICKLER SYNDROME | Semantic Scholar
Stickler Marshall Syndrome: Adelaide boy with rare genetic condition living mainstream life with specialist intervention | The Advertiser
Facial Photographs of patients with deletions in the COL11A1 gene. Two... | Download Scientific Diagram