Coffin Siris Syndrome
Nov. 5, 2024
Coffin-Siris syndrome: MedlinePlus Genetics Maternal transmission of a mild Coffin–Siris syndrome phenotype caused by a SOX11 missense variant | European Journal of Human Genetics Coffin–Siris syndrome - Wikipedia Coffin–Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene | European Journal of Human Genetics Coffin–Siris Syndrome and the BAF Complex: Genotype–Phenotype Study in 63 Patients - Santen - 2013 - Human Mutation - Wiley Online Library Clinical features, diagnostic criteria, and management of Coffin–Siris syndrome - Vergano - 2014 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library | Coffin Siris Syndrome
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![Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2021;26:227-231]](https://www.hkjpaed.org/figure/2021;26;227-231-fig1.jpg){kind=link}
![PDF] Coffin-Siris Syndrome in Two Sisters in Nepal | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/defe42309554873234489d69f8d562f889aa959c/2-Figure2-1.png){kind=link}
![PDF] Coffin-Siris Syndrome in Two Sisters in Nepal | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/defe42309554873234489d69f8d562f889aa959c/2-Figure3-1.png){kind=link}
![PDF] A case of Coffin–Siris syndrome with severe congenital heart disease and a nov…](https://d3i71xaburhd42.cloudfront.net/d76cd4b8c0483d25db0cd6e863143b27c263c436/3-Figure1-1.png){kind=link}
