Publication: Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
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Abstract
Congenital heart disease (CHD) affecting the conotruncal region of the heart, occurs in 40-50% of patients with 22q11.2 deletion syndrome (22q11.2DS). This syndrome is a rare disorder with relative ge...
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García, Sixto; Fernández, Luis; Zhang, Zhengdong; Goldmuntz, Elizabeth; Gu, Raquel; Emanuel, Beverly; Zheng, Deyou; Marshal, Christian; Basset,Anne; Wang, Tao; Morrow, Bernice,
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