Journal of Pediatric Genetics

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Pendleton, K. E., Hernandez-Garcia, A., Lyu, J. M., Campbell, I. M., Shaw, C. A., Vogt, J., High, F. A., Donahoe, P. K., Chung, W. K., & Scott, D. A. (2023). FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia. Journal of Pediatric Genetics, 13(01), 029–034. CLOCKSS. https://doi.org/10.1055/s-0043-1767731
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