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

enthalten in: PLoS genetics | 2017

von Racedo, S. | Hasten, E. | Lin, M. | +6

Tbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of mastication

enthalten in: Human molecular genetics | 2014

von Kong, P. | Racedo, S. | Macchiarulo, S. | +6

Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients

enthalten in: American journal of medical genetics. Part A | 2012

von Herman, S. | Guo, T. | McGinn, D. | +31

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients

enthalten in: Human mutation | 2011

von Guo, T. | McDonald-McGinn, D. | Blonska, A. | +31