Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 2 of 2 for “"Stickler syndrome"”.
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Hereditary progressive arthro-opthalmopathy (Stickler Syndrome): a clinical analysis and search for linkage
This document only includes an excerpt of the corresponding thesis or dissertation. To request a digital scan of the full text, please contact the Ruth Lilly Medical Library's Interlibrary Loan Department (rlmlill@iu.edu).
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Genetic, Cellular and Ultrastructural Mechanisms in Retinal Detachment
… – genetic, ultrastructural and transcriptomic. Stickler syndrome is the most common form of hereditary RRD, usually from dominant variants in genes for type II and XI collagen. Here, two pedigrees with atypical mutation patterns are investigated. One family had a heterozygous *BMP4* variant …