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Genome Medicine
|
October 7, 2010
Genetically complex epilepsies, copy number variants and syndrome constellations
Heather C Mefford, John C Mulley
Current Opinion in Neurology
|
January 22, 2011
Genetic contribution to common epilepsies
Sanjay M Sisodiya, Heather C Mefford
Current Opinion in Genetics & Development
|
November 26, 2022
Editorial overview: Congenital cardiovascular disease
Neil A Hanchard, Heather C Mefford
Epilepsia
|
January 29, 2011
Epilepsy and the new cytogenetics
John C Mulley, Heather C Mefford
Journal of Pediatric Genetics
|
September 13, 2016
Next-Generation Sequencing in Intellectual Disability
Gemma L Carvill, Heather C Mefford
Methods in Molecular Biology (Clifton, N.J.)
|
August 9, 2011
Detection of copy number variation using SNP genotyping
Gregory M Cooper, Heather C Mefford
Nature Reviews. Neurology
|
August 13, 2014
Epilepsy: Beyond the single nucleotide variant in epilepsy genetics
Ingrid E Scheffer, Heather C Mefford
The New England Journal of Medicine
|
March 4, 2026
Toward a Disease-Modifying Therapy for Dravet Syndrome
Gemma L Carvill, Heather C Mefford
Epilepsy & Behavior : E&B
|
October 5, 2013
Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Epilepsy & Behavior : E&B
|
June 13, 2013
The unexpected role of copy number variations in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Page
of 23
Search research articles
Search
Showing results (21-30 of 222) with videos related to
Sort By:
Page
of 23
Genome Medicine
|
October 7, 2010
Genetically complex epilepsies, copy number variants and syndrome constellations
Heather C Mefford, John C Mulley
Current Opinion in Neurology
|
January 22, 2011
Genetic contribution to common epilepsies
Sanjay M Sisodiya, Heather C Mefford
Current Opinion in Genetics & Development
|
November 26, 2022
Editorial overview: Congenital cardiovascular disease
Neil A Hanchard, Heather C Mefford
Epilepsia
|
January 29, 2011
Epilepsy and the new cytogenetics
John C Mulley, Heather C Mefford
Journal of Pediatric Genetics
|
September 13, 2016
Next-Generation Sequencing in Intellectual Disability
Gemma L Carvill, Heather C Mefford
Methods in Molecular Biology (Clifton, N.J.)
|
August 9, 2011
Detection of copy number variation using SNP genotyping
Gregory M Cooper, Heather C Mefford
Nature Reviews. Neurology
|
August 13, 2014
Epilepsy: Beyond the single nucleotide variant in epilepsy genetics
Ingrid E Scheffer, Heather C Mefford
The New England Journal of Medicine
|
March 4, 2026
Toward a Disease-Modifying Therapy for Dravet Syndrome
Gemma L Carvill, Heather C Mefford
Epilepsy & Behavior : E&B
|
October 5, 2013
Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Epilepsy & Behavior : E&B
|
June 13, 2013
The unexpected role of copy number variations in juvenile myoclonic epilepsy
Ingo Helbig, Corinna Hartmann, Heather C Mefford
Page
of 23