Browse by Journal Title

2015

CCN1 mutation is associated with atrial septal defect.
Perrot, A., Schmitt, K.R., Roth, E.M., Stiller, B., Posch, M.G., Browne, E.N.L., Timmann, C., Horstmann, R.D., Berger, F. and Ozcelik, C.
Pediatric Cardiology 36 (2): 295-299. February 2015

2009

Developmental signaling in myocardial progenitor cells: A comprehensive view of Bmp- and Wnt/beta-catenin signaling.
Klaus, A. and Birchmeier, W.
Pediatric Cardiology 30 (5): 609-616. July 2009

2006

Mutations in the EGF-CFC gene Cryptic are an infrequent cause of congenital heart disease.
Oezcelik, C., Bit-Avragim, N., Panek, A., Gaio, U., Geier, C., Lange, P.E., Dietz, R., Posch, M.G., Perrot, A. and Stiller, B.
Pediatric Cardiology 27 (6): 695-698. December 2006