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Philip Holmgren

Showing results (1-10 of 7) with videos related to

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Neurology|September 20, 2013
Duplications of 17q12 can cause familial fever-related epilepsy syndromesKatia Hardies, Sarah Weckhuysen, Elke Peeters, et al.
Scientific Reports|January 27, 2023
Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotypingEwa Sieliwonczyk, Bert Vandendriessche, Charlotte Claes, et al.
Prenatal Diagnosis|June 14, 2016
Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal testKatrien Janssens, Kathleen Deiteren, Anke Verlinden, et al.
BMC Research Notes|May 5, 2016
Improving Care And Research Electronic Data Trust Antwerp (iCAREdata): a research database of linked data on out-of-hours primary careAnnelies Colliers, Stefaan Bartholomeeusen, Roy Remmen, et al.
Epilepsia|February 16, 2013
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriersSarah Weckhuysen, Philip Holmgren, Rik Hendrickx, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2013
PRRT2 mutations: exploring the phenotypical boundariesTania Djémié, Sarah Weckhuysen, Philip Holmgren, et al.
Prenatal Diagnosis|October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Neurology|September 20, 2013
Duplications of 17q12 can cause familial fever-related epilepsy syndromesKatia Hardies, Sarah Weckhuysen, Elke Peeters, et al.
Scientific Reports|January 27, 2023
Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotypingEwa Sieliwonczyk, Bert Vandendriessche, Charlotte Claes, et al.
Prenatal Diagnosis|June 14, 2016
Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal testKatrien Janssens, Kathleen Deiteren, Anke Verlinden, et al.
BMC Research Notes|May 5, 2016
Improving Care And Research Electronic Data Trust Antwerp (iCAREdata): a research database of linked data on out-of-hours primary careAnnelies Colliers, Stefaan Bartholomeeusen, Roy Remmen, et al.
Epilepsia|February 16, 2013
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriersSarah Weckhuysen, Philip Holmgren, Rik Hendrickx, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2013
PRRT2 mutations: exploring the phenotypical boundariesTania Djémié, Sarah Weckhuysen, Philip Holmgren, et al.
Prenatal Diagnosis|October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Pageof 1