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oesophageal atresia
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Genetic Markers
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No genes found
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OMIM - Congenital disorder
OMIM - VATER association
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Abnormal control of lung branching in experimental esophageal atresia.
EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia.
Mutational analysis of NOG in esophageal atresia and tracheoesophageal fistula patients.
Postoperative appearances of esophageal atresia repair: retrospective study of 210 patients with rev…
Why gastric perforation occurs in patients with isolated esophageal atresia: more vulnerable stomach…
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Study in Children With the Diagnosis of Congenital Diaphragmatic Hernia (CDH) and Oesophageal Atresi…
Use of Indocyanine Green During Primary Repair of Oesophageal Atresia and Distal Tracheo-oesophageal…
National Register of Oesophageal Atresia
Swallowing, Feeding and Eating in Children Born With Oesophageal Atresia/Trache-oesophageal Fistula …
Study of the Effect of the Time of Diagnosis (Antenatal vs. Postnatal) on the Post-traumatic Reactio…
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