Fetal Diagnosis of Supravalvular Aortic Stenosis and Pulmonary Stenosis in a Family with Non-Syndromic Elastin Mutation
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00246-024-03418-8.pdf
Reference9 articles.
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2. Pober BR, Johnson M, Urban Z (2008) Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome. J Clin Invest 118:1606–1615. https://doi.org/10.1172/JCI35309
3. Li F-F, Chen W-J, Yao D et al (2022) Clinical phenotypes study of 231 children with Williams syndrome in China: a single-center retrospective study. Mol Genet Genomic Med 10:e2069. https://doi.org/10.1002/mgg3.2069
4. Cha SG, Song MK, Lee SY et al (2019) Long-term cardiovascular outcome of Williams syndrome. Congenit Heart Dis 14:684–690. https://doi.org/10.1111/chd.12810
5. Hayano S, Okuno Y, Tsutsumi M et al (2019) Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis. Int J Cardiol 274:290–295. https://doi.org/10.1016/j.ijcard.2018.09.032
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