Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits, and possibly Diamond-Blackfan anemia

по Wat, Margaret J., Enciso, Victoria B., Wiszniewski, Wojciech, Resnick, Trevor, Bader, Patricia, Roeder, Elizabeth R., Freedenberg, Debra, Brown, Chester, Stankiewicz, Pawel, Cheung, Sau-Wai, Scott, Daryl A.
Опубликовано 2010

Chromosome 8p23.1 Deletions as a Cause of Complex Congenital Heart Defects and Diaphragmatic Hernia

по Wat, Margaret J., Shchelochkov, Oleg A., Holder, Ashley M., Breman, Amy M., Dagli, Aditi, Bacino, Carlos, Scaglia, Fernando, Zori, Roberto T., Cheung, Sau Wai, Scott, Daryl A., Kang, Sung-Hae Lee
Опубликовано 2009

Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1

по Wat, Margaret J., Beck, Tyler F., Hernández-García, Andrés, Yu, Zhiyin, Veenma, Danielle, Garcia, Monica, Holder, Ashley M., Wat, Jeanette J., Chen, Yuqing, Mohila, Carrie A., Lally, Kevin P., Dickinson, Mary, Tibboel, Dick, de Klein, Annelies, Lee, Brendan, Scott, Daryl A.
Опубликовано 2012

Genomic Alterations that Contribute to the Development of Isolated and Non-Isolated Congenital Diaphragmatic Hernia

по Wat, Margaret J., Veenma, Danielle, Hogue, Jacob, Holder, Ashley M., Yu, Zhiyin, Wat, Jeanette, Hanchard, Neil, Shchelochkov, Oleg A., Fernandes, Caraciolo J., Johnson, Anthony, Lally, Kevin P., Slavotinek, Anne, Danhaive, Olivier, Schaible, Thomas, Cheung, Sau-Wai, Rauen, Katherine A., Tonk, Vijay S., Tibboel, Dick, de Klein, Annelies, Scott, Daryl A.
Опубликовано 2011