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Article

Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia

21 Oct 2022

Abstract excerpt

Developmental abnormalities provide a unique opportunity to seek for the molecular mechanisms underlying human organogenesis. Esophageal development remains incompletely understood and elucidating causes for esophageal atresia (EA) in humans would contribute to achieve a better comprehension. Prenatal detection, syndromic classification, molecular diagnosis, and prognostic factors in EA are challenging. Some...

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PMID: 36271508
DOI: 10.1002/ajmg.a.62989

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