Morten Dunø
Department of Clinical Genetics
University of Copenhagen
Rigshospitalet
Copenhagen
Denmark
Name/email consistency: high
- High-resolution melting facilitates mutation screening of PYGM in patients with McArdle disease. Duno, M., Quinlivan, R., Vissing, J., Schwartz, M. Ann. Hum. Genet. (2009)
- cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark. Duno, M., Sveen, M.L., Schwartz, M., Vissing, J. Eur. J. Hum. Genet. (2008)
- Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patients. Duno, M., Skovby, F., Schwartz, M. Ann. Hum. Genet. (2007)
- Difference in allelic expression of the CLCN1 gene and the possible influence on the myotonia congenita phenotype. Dunø, M., Colding-Jørgensen, E., Grunnet, M., Jespersen, T., Vissing, J., Schwartz, M. Eur. J. Hum. Genet. (2004)
- Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion. Dunø, M., Hove, H., Kirchhoff, M., Devriendt, K., Schwartz, M. Hum. Genet. (2004)
