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Petra M C Callenbach

Showing results (21-30 of 26) with videos related to

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Neurology|October 19, 2012
PRRT2 mutation causes benign familial infantile convulsionsBoukje de Vries, Petra M C Callenbach, Jessica T Kamphorst, et al.
Epilepsia|September 27, 2003
Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22qPetra M C Callenbach, Arn M J M van den Maagdenberg, Jouke J Hottenga, et al.
Neurology|November 12, 2017
δ-Catenin (<i>CTNND2</i>) missense mutation in familial cortical myoclonic tremor and epilepsyAnne-Fleur van Rootselaar, Alexander J Groffen, Boukje de Vries, et al.
European Journal of Medical Genetics|August 21, 2018
PRRT2-related phenotypes in patients with a 16p11.2 deletionDanique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
Brain : a Journal of Neurology|December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotypeVincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Neurology|October 19, 2012
PRRT2 mutation causes benign familial infantile convulsionsBoukje de Vries, Petra M C Callenbach, Jessica T Kamphorst, et al.
Epilepsia|September 27, 2003
Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22qPetra M C Callenbach, Arn M J M van den Maagdenberg, Jouke J Hottenga, et al.
Neurology|November 12, 2017
δ-Catenin (<i>CTNND2</i>) missense mutation in familial cortical myoclonic tremor and epilepsyAnne-Fleur van Rootselaar, Alexander J Groffen, Boukje de Vries, et al.
European Journal of Medical Genetics|August 21, 2018
PRRT2-related phenotypes in patients with a 16p11.2 deletionDanique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, et al.
Brain : a Journal of Neurology|December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotypeVincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Pageof 3