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Retinopathy and bone marrow failure revealing Coats plus syndrome | BMJ Case Reports
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![PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/907bce1bf580cae0aeeede165c065630280da1ab/3-Figure1-1.png "PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar")
PDF] Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects | Semantic Scholar
PDF) Retinopathy and bone marrow failure revealing Coats plus syndrome | Paula Kjöllerström - Academia.edu
Coats-plus syndrome: when imaging leads to genetic diagnosis | BMJ Case Reports
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Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
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Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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