Major Chromosomal Abnormalities and Necrotizing Enterocolitis: Is there a Link?
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Publisher
Jaypee Brothers Medical Publishing
Link
https://www.newbornjournal.org/doi/pdf/10.5005/jp-journals-11002-0032
Reference24 articles.
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2. 2. Verma IC, Puri RD. Global burden of genetic disease and the role of genetic screening. Semin Fetal Neonatal Med 2015;20(5):354–363. DOI: 10.1016/j.siny.2015.07.002.
3. 3. Cuna A, George L, Sampath V. Genetic predisposition to necrotizing enterocolitis in premature infants: current knowledge, challenges, and future directions. Semin Fetal Neonatal Med 2018;23(6):387–393. DOI: 10.1016/j.siny.2018.08.006.
4. 4. Good M, Chu T, Shaw P, et al. Global hypermethylation of intestinal epithelial cells is a hallmark feature of neonatal surgical necrotizing enterocolitis. Clin Epigenetics 2020;12(1):190. DOI: 10.1186/s13148-020-00983-6.
5. 5. Jilling T, Ambalavanan N, Cotten CM, et al. Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8. Pediatr Res 2018;83(5):943–953. DOI: 10.1038/pr.2018.33.
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