Group by:
Date |
Item TypeArticle
CCN1 mutation is associated with atrial septal defect.
Perrot, A.
ORCID: https://orcid.org/0000-0002-8800-342X, 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
Developmental signaling in myocardial progenitor cells: A comprehensive view of Bmp- and Wnt/beta-catenin signaling.
Klaus, A.
ORCID: https://orcid.org/0000-0002-1164-3322 and Birchmeier, W.
ORCID: https://orcid.org/0000-0003-1173-0829
Pediatric Cardiology 30
(5): 609-616.
July 2009
Mutations in the EGF-CFC gene Cryptic are an infrequent cause of congenital heart disease.
Oezcelik, C., Bit-Avragim, N.
ORCID: https://orcid.org/0000-0003-4606-1899, Panek, A., Gaio, U., Geier, C.
ORCID: https://orcid.org/0000-0001-5281-8187, Lange, P.E., Dietz, R., Posch, M.G., Perrot, A.
ORCID: https://orcid.org/0000-0002-8800-342X and Stiller, B.
Pediatric Cardiology 27
(6): 695-698.
December 2006
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