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Correspondence
A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death
- Correspondence to Dr Gabriela Jones, Leicester Clinical Genetics Department, University Hospitals Leicester NHS Trust, Leicester, LE1 5WW; gabriela.jones{at}uhl-tr.nhs.uk
Citation
A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death
Publication history
- Received July 19, 2013
- Revised September 30, 2013
- Accepted October 10, 2013
- First published November 4, 2013.
Online issue publication
June 14, 2020
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