Global DNA Methylation as a Potential Underlying Mechanism of Congenital Disease Development
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IntechOpen
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http://www.intechopen.com/download/pdf/70871
Reference144 articles.
1. WHO. Available from: https://www.who.int/news-room/fact-sheets/detail/congenital-anomalies
2. Morris JK, Springett AL, Greenlees R, Loane M, Addor MC, Arriola L, et al. Trends in congenital anomalies in Europe from 1980 to 2012. PLoS ONE. 2018;13(4):e0194986. DOI: 10.1371/journal.pone.0194986
3. Chowdhury S, Erickson SW, MacLeod SL, Cleves MA, Hu P, Karim MA, et al. Maternal genome-wide DNA methylation patterns and congenital heart defects. PLoS ONE. 2011;6(1):e16506. DOI: 10.1371/journal.pone.0016506
4. Chowdhury S, Cleves MA, MacLeod SL, James SJ, Zhao W, Hobbs CA. Maternal DNA hypomethylation and congenital heart defects. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2011;91:69-76. DOI: 10.1002/bdra.20761
5. Babić Božović I, Stanković A, Živković M, Vraneković J, Mahulja-Stamenković V, et al. Maternal LINE-1 DNA methylation and congenital heart defects in down syndrome. Frontiers in Genetics. 2019;10:41. DOI: 10.3389/fgene.2019.00041
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