Mauro Longoni
2PUBLICATIONS
6CO-AUTHORS
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Publications (2)
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|Dec 12, 2018
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.Hongjian Qi, Lan Yu, Xueya Zhou
|Mar 18, 2017
Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia.Mauro Longoni, Frances A High, Hongjian Qi
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