Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
Abstract Background Oesophageal atresia (OA) is a life-threatening developmental defect characterized by a lost continuity between the upper and lower oesophagus. The most common form is a distal connection between the trachea and the oesophagus, i.e. a tracheoesophageal fistula (TEF). The condition...
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| Main Authors: | , , , , , |
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| Format: | Book |
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BMC,
2020-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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