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Updated: May 9, 2026

Conditional Reprogramming of Pediatric Human Esophageal Epithelial Cells for Use in Tissue Engineering and Disease Investigation
Published on: March 22, 2017
Chromosome aberrations and gene mutations in patients with esophageal atresia
Damian Bednarczyk1, Maria M Sasiadek, Robert Smigiel
1Department of Genetics, Wroclaw Medical University, Wroclaw, Poland.
Abstract:
Esophageal atresia (EA) is one of the most frequent congenital malformations of the gastrointestinal tract. Many genetic alterations in patients with EA have been described in the literature. It is thought that the etiology of EA is heterogeneous. This review of the literature provides detailed information about chromosomal aberrations, gene mutations, and clinical features of neonates with EA, and serves as an excellent source to compare newly diagnosed patients with those described in the literature.
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