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Publication: Wang et al., 2019 - Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases
All Figures: Figures for Wang et al., 2019

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FIGURE 1

De novo mutations (DNMs) validation of selected seven DNVs in trios affected with anencephaly. Chromatograms of the three individuals from one trio (from top to bottom: fetus, father, and mother). (A) BRF1 de novo variant. (B) CNOT3 de novo variant. (C) DMXL2 de novo variant. (D) ORC3 de novo variant. (E) SATB2 de novo variant. (F) SHPRH de novo variant. (G) WIPI1 de novo variant.

Acknowledgments

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