Erica Hasten
2PUBLICATIONS
4CO-AUTHORS
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Publications (2)
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|Aug 15, 2019
Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome.Erica Hasten, Bernice E Morrow
|Mar 28, 2017
Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.Silvia E Racedo, Erica Hasten, Mingyan Lin
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