Browse by Journal Title

2015

Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome.
Kuechler, A., Altmüller, J., Nürnberg, P., Kotthoff, S., Kubisch, C. and Borck, G.
Molecular and Cellular Probes 29 (5): 330-334. October 2015

2000

Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
Haug, K., Kremerskothen, J., Hallmann, K., Sander, T., Dullinger, J., Rau, B., Beyenburg, S., Lentze, M.J., Barnekow, A., Elger, C.E., Propping, P. and Heils, A.
Molecular and Cellular Probes 14 : 255-260. 1 August 2000