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Chromatin Regulators in the TBX1 Network Confer Risk for Conotruncal Heart Defects in 22Q11.2ds

Yingjie Zhao,Yujue Wang,Lijie Shi,Donna M. McDonald-McGinn,T. Blaine Crowley,Daniel E. McGinn,Oanh T. Tran,Daniella Miller,Jhih-Rong Lin,Elaine Zackai,H. Richard Johnston,Eva W. C. Chow,Jacob A. S. Vorstman,Claudia Vingerhoets,Therese van Amelsvoort,Doron Gothelf,Ann Swillen,Jeroen Breckpot,Joris R. Vermeesch,Stephan Eliez,Maude Schneider,Marianne B. M. van den Bree,Michael J. Owen,Wendy R. Kates,Gabriela M. Repetto,Vandana Shashi,Kelly Schoch,Carrie E. Bearden,M. Cristina Digilio,Marta Unolt,Carolina Putotto,Bruno Marino,Maria Pontillo,Marco Armando,Stefano Vicari,Kathleen Angkustsiri,Linda Campbell,Tiffany Busa,Damian Heine-Suñer,Kieran C. Murphy,Declan Murphy,Sixto García-Miñaúr,Luis Fernández,Zhengdong D. Zhang,Elizabeth Goldmuntz,Raquel E. Gur,Beverly S. Emanuel,Deyou Zheng,Christian R. Marshall,Anne S. Bassett,Tao Wang,Bernice E. Morrow

NPJ GENOMIC MEDICINE（2023）

Cited 2|Views67
Key words
Congenital heart defects,Development,Biomedicine,general,Human Genetics,Internal Medicine,Bioinformatics,Gene Therapy,Gene Function
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