Jong, E.M. de

patient anomaly ea /tef atresia syndrome defect esophageal atresia vacterl vacterl association association esophageal study deletion genet mutation stula factor number tracheoesophageal fi stula development oesophageal atresia guideline liver foregut tracheo-oesophageal fi stula malformations chromosomal genetic infant chapter analysis subset birth oesophageal chromosome phenotype signi psoriasis journal tracheoesophageal model polyalanine region brosi abnormality pediatr spectrum speci zic 3 gene tracheal agenesis agenesi table tracheo-esophageal fi stula diagnosis heterotaxy result vacterl spectrum dermatologist pregnancy liver fi brosis signi ficantly copy number variations addition tracheal x-linked heterotaxy j med genet felix cause biopsy tracheo-esophageal variation foregut development expansion trachea anal atresia postnatal esophagus heart disease x-linked