Papers: 10.1371/journal.pgen.1007822

https://doi.org/10.1371/journal.pgen.1007822

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Cited by: 74
Author(s): Hongjian Qi, Lan Yu, Xueya Zhou, Julia Wynn, Haoquan Zhao, Yicheng Guo, Na Zhu, Alexander Kitaygorodsky, Rebecca Hernan, Guðrún Aspelund, Foong‐Yen Lim, Timothy M. Crombleholme, Robert A. Cusick, Kenneth S. Azarow, Melissa E. Danko, Dai H. Chung, Brad W. Warner, George B. Mychaliska, Douglas A. Potoka, Amy J. Wagner, Mahmoud Elfiky, Jay M. Wilson, Debbie Nickerson, Michael J. Bamshad, Frances A. High, Mauro Longoni, Patricia K. Donahoe, Wendy K. Chung, Yufeng Shen
Published: almost 8 years ago

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