Cite
Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1
MLA
Mariya R. Ahmed, et al. “Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1.” Genes, vol. 13, no. 3, Feb. 2022, p. 411. EBSCOhost, https://doi.org/10.3390/genes13030411.
APA
Mariya R. Ahmed, Saumil Sethna, Laura A. Krueger, Michael B. Yang, & Robert B. Hufnagel. (2022). Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1. Genes, 13(3), 411. https://doi.org/10.3390/genes13030411
Chicago
Mariya R. Ahmed, Saumil Sethna, Laura A. Krueger, Michael B. Yang, and Robert B. Hufnagel. 2022. “Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1.” Genes 13 (3): 411. doi:10.3390/genes13030411.