Roselie J. Jongbloed
Department of Genetics and Cell Biology
University Maastricht
Maastricht
Netherlands
Name/email consistency: high
- Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy. Jongbloed, R.J., Marcelis, C.L., Doevendans, P.A., Schmeitz-Mulkens, J.M., Van Dockum, W.G., Geraedts, J.P., Smeets, H.J. J. Am. Coll. Cardiol. (2003)
- DHPLC analysis of potassium ion channel genes in congenital long QT syndrome. Jongbloed, R., Marcelis, C., Velter, C., Doevendans, P., Geraedts, J., Smeets, H. Hum. Mutat. (2002)









