FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia

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
Authors:
Katherine E Pendleton
Andres Hernandez-Garcia
Jennifer M Lyu
Ian M Campbell
Chad A Shaw
Julie Vogt
Frances A High
Patricia K Donahoe
Wendy K Chung
Daryl A Scott
Affiliated Authors:
Wendy K Chung
Author Keywords:
cdh
foxp1
foxp2
foxp3
foxp4
Publication Type:
Article
Unique ID:
10.1055/s-0043-1767731
PMID:
Publication Date:
Data Source:
PubMed

Record Created: