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Stickler syndrome: Clinical characteristics and diagnostic criteria - Rose - 2005 - American Journal of Medical Genetics Part A - Wiley Online Library
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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
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Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the α2(XI) chain of type XI collagen - ScienceDirect
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Genetic syndromes screening by facial recognition technology: VGG-16 screening model construction and evaluation | Orphanet Journal of Rare Diseases | Full Text
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Therapeutic and diagnostic advances in Stickler syndrome - Martin Snead, Howard Martin, Peter Bale, Nick Shenker, David Baguley, Philip Alexander, Annie McNinch, Arabella Poulson, 2020
Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation - Brizola - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Stickler Syndrome Corey Thompson. Stickler Syndrome Stickler Syndrome is a genetic disorder that affects the collagen which connects tissues, bones, and. - ppt download
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The author/presenter has no conflict of interest nor financial interest regarding any content within this presentation.
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