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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.
Am J Hum Genet. 2023 Oct 5;110(10):1787-1803. doi: 10.1016/j.ajhg.2023.09.002. Epub 2023 Sep 25.
Am J Hum Genet. 2023.
PMID: 37751738
Free PMC article.
Congenital diaphragmatic hernias: from genes to mechanisms to therapies.
Kardon G, Ackerman KG, McCulley DJ, Shen Y, Wynn J, Shang L, Bogenschutz E, Sun X, Chung WK.
Kardon G, et al.
Dis Model Mech. 2017 Aug 1;10(8):955-970. doi: 10.1242/dmm.028365.
Dis Model Mech. 2017.
PMID: 28768736
Free PMC article.
Review.
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Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias.
Bogenschutz EL, Fox ZD, Farrell A, Wynn J, Moore B, Yu L, Aspelund G, Marth G, Yandell M, Shen Y, Chung WK, Kardon G.
Bogenschutz EL, et al.
HGG Adv. 2020 Oct 22;1(1):100008. doi: 10.1016/j.xhgg.2020.100008. Epub 2020 Aug 25.
HGG Adv. 2020.
PMID: 33263113
Free PMC article.
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Cell culture system to assay candidate genes and molecular pathways implicated in congenital diaphragmatic hernias.
Bogenschutz EL, Sefton EM, Kardon G.
Bogenschutz EL, et al.
Dev Biol. 2020 Nov 1;467(1-2):30-38. doi: 10.1016/j.ydbio.2020.07.013. Epub 2020 Aug 19.
Dev Biol. 2020.
PMID: 32827499
Free PMC article.
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