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I E Scheffer

Showing results (71-80 of 75) with videos related to

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Neurology|July 15, 2011
De novo SCN1A mutations in migrating partial seizures of infancyD Carranza Rojo, L Hamiwka, J M McMahon, et al.
Epilepsy Research|February 16, 2010
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysisC G F de Kovel, D Pinto, U Tauer, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Neurology|July 15, 2011
De novo SCN1A mutations in migrating partial seizures of infancyD Carranza Rojo, L Hamiwka, J M McMahon, et al.
Epilepsy Research|February 16, 2010
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysisC G F de Kovel, D Pinto, U Tauer, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.
Pageof 8