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Familiality and molecular genetics of attention networks in ADHD.
Konrad, K. and Dempfle, A. and Friedel, S. and Heiser, P. and Holtkamp, K. and Walitza, S. and Sauer, S. and Warnke, A. and Remschmidt, H. and Gilsbach, S. and Schäfer, H. and Hinney, A. and Hebebrand, J. and Herpertz-Dahlmann, B.
American Journal of Medical Genetics B 153B (1): 148-158. 5 January 2010


Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus-Merzbacher-like leukodystrophy.
Ruf, N. and Martelli, M. and Weschke, B. and Uhlenberg, B.
American Journal of Medical Genetics B 144 (3): 365-366. 5 April 2007

Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.
Lorenz, S. and Heils, A. and Kasper, J.M. and Sander, T.
American Journal of Medical Genetics B 144B (1): 10-13. 5 January 2007


Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder.
Lohoff, F.W. and Sander, T. and Ferraro, T.N. and Dahl, J.P. and Gallinat, J. and Berrettini, W.H.
American Journal of Medical Genetics B 139 (1): 51-53. 5 November 2005


Candidate gene analysis of the human metabotropic glutamate receptor type 4 (GRM4) in patients with juvenile myoclonic epilepsy.
Izzi, C. and Barbon, A. and Toliat, M.R. and Heils, A. and Becker, C. and Nuernberg, P. and Sander, T. and Barlati, S.
American Journal of Medical Genetics B 123B (1): 59-63. 15 November 2003

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