CHRND variant in a paternally inherited esophageal atresia and tracheoesophgageal fistula: Report of a case
Article in Birth Defects Research (December 2023)
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First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
Article in Human Genetics and Genomics Advances (January 2022)