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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).

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001006092 10
Publications Citations
Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants.
BMC Med Genomics 13: 2020 85