Retinopathy and bone marrow failure revealing Coats plus syndrome | BMJ Case Reports
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene. | Semantic Scholar
Coats Plus Syndrome and Mutation of the TERT Gene: A Case Report
Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology
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Coats plus syndrome: MedlinePlus Genetics
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Quid du syndrome de Coats plus ? - Réalités Ophtalmologiques
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Genes | Free Full-Text | Patient-Derived iPSCs Reveal Evidence of Telomere Instability and DNA Repair Deficiency in Coats Plus Syndrome
Coats Plus : la version systémique de la maladie de Coats - ScienceDirect
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics
Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children – a case report | BMC Pediatrics | Full Text
India diagnoses first case of Coats plus syndrome | Mint
Retinopathy and bone marrow failure revealing Coats plus syndrome | BMJ Case Reports
![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
Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
Coats Disease: Treatment, Stages, and Symptoms
Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children – a case report | BMC Pediatrics | Full Text
