Journal
PLoS Genetics
Publication Date
2018
Volume
14
Issue
12
Inclusive Pages
e1007822
Document Type
Open Access Publication
DOI
10.1371/journal. pgen.1007822
Rights and Permissions
Qi H, Yu L, Zhou X, Wynn J, Zhao H, et al. (2018) De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders. PLOS Genetics 14(12): e1007822. https://doi.org/10.1371/journal.pgen.1007822
Recommended Citation
Warner, Brad W. and et al., "De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders." PLoS Genetics. 14, 12. e1007822. (2018).
https://digitalcommons.wustl.edu/open_access_pubs/7731
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Figure S1.pdf (569 kB)
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Figure S2.pdf (730 kB)
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Figure S3.pdf (1345 kB)
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Figure S4.pdf (958 kB)
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Figure S5.pdf (656 kB)
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Figure S6.pdf (459 kB)
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Figure S7.pdf (422 kB)
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Figure S8.pdf (374 kB)
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Figure S9.pdf (398 kB)
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Table S1.pdf (233 kB)
Table S1
Table S2.pdf (521 kB)
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Table S3.pdf (319 kB)
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Table S4.pdf (263 kB)
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Table S5.pdf (643 kB)
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Table S6.pdf (283 kB)
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Table S7.pdf (297 kB)
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Text S1.pdf (253 kB)
Text S1
