Genome sequencing of oesophagus atresia families
To gain insight into gene variants and genes associated with isolated Oesophageal atresia (OA) we conducted whole genome sequencing on samples from three families with recurrent cases affected by congenital and isolated tracheoesophageal fistula (TEF).
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants.
BMC Med Genomics 13: 2020 85