Obermeier, T.
University Hospital Schleswig-Holstein
2 papers on CoChat
Most cited papers
- Verified
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
de Kovel, C. G. F., Trucks, H., Helbig, I., Mefford, H. C., Baker, C., Leu, C., Kluck, C., Muhle, H., von Spiczak, S., Ostertag, P., et al. (2010) · Brain
Genomic variations and chromosomal abnormalitiesEpilepsy research and treatment
Cited by 445
- Verified
Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies
Jähn, J. A., von Spiczak, S., Muhle, H., Obermeier, T., Franke, A., Mefford, H. C., Stephani, U., & Helbig, I. (2014) · Epilepsy Research
Epilepsy research and treatmentGenomic variations and chromosomal abnormalities
Cited by 26
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