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Guy Froyen

Showing results (1-10 of 77) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 17, 2019
Clinical Validation of Targeted Solid Tumor ProfilingGuy Froyen, Brigitte Maes
Journal of Cellular and Molecular Medicine|November 28, 2006
X-linked mental retardation and epigeneticsGuy Froyen, Marijke Bauters, Thierry Voet, et al.
European Journal of Medical Genetics|September 24, 2005
X chromosome array-CGH for the identification of novel X-linked mental retardation genesMarijke Bauters, Hilde Van Esch, Peter Marynen, et al.
Cancers|May 28, 2022
Diagnostic Validation of a Comprehensive Targeted Panel for Broad Mutational and Biomarker Analysis in Solid TumorsGuy Froyen, Ellen Geerdens, Severine Berden, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genesHilde Van Esch, Anna Jansen, Marijke Bauters, et al.
American Journal of Medical Genetics|October 12, 2002
Clinical study and haplotype analysis in two brothers with Partington syndromeSuzanna G M Frints, Martine Borghgraef, Guy Froyen, et al.
Cancers|June 22, 2023
Liquid Biopsy in Early-Stage Lung Cancer: Current and Future Clinical ApplicationsOlivia Vandekerckhove, Kristof Cuppens, Karin Pat, et al.
BMC Medical Genomics|December 21, 2018
Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disabilityAlena Zablotskaya, Hilde Van Esch, Kevin J Verstrepen, et al.
American Journal of Medical Genetics|October 12, 2002
Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndromeSuzanna G M Frints, Guy Froyen, Peter Marynen, et al.
Frontiers in Behavioral Neuroscience|July 29, 2015
Nxf7 deficiency impairs social exploration and spatio-cognitive abilities as well as hippocampal synaptic plasticity in miceZsuzsanna Callaerts-Vegh, Tariq Ahmed, Ben Vermaercke, et al.
Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
Methods in Molecular Biology (Clifton, N.J.)|January 17, 2019
Clinical Validation of Targeted Solid Tumor ProfilingGuy Froyen, Brigitte Maes
Journal of Cellular and Molecular Medicine|November 28, 2006
X-linked mental retardation and epigeneticsGuy Froyen, Marijke Bauters, Thierry Voet, et al.
European Journal of Medical Genetics|September 24, 2005
X chromosome array-CGH for the identification of novel X-linked mental retardation genesMarijke Bauters, Hilde Van Esch, Peter Marynen, et al.
Cancers|May 28, 2022
Diagnostic Validation of a Comprehensive Targeted Panel for Broad Mutational and Biomarker Analysis in Solid TumorsGuy Froyen, Ellen Geerdens, Severine Berden, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genesHilde Van Esch, Anna Jansen, Marijke Bauters, et al.
American Journal of Medical Genetics|October 12, 2002
Clinical study and haplotype analysis in two brothers with Partington syndromeSuzanna G M Frints, Martine Borghgraef, Guy Froyen, et al.
Cancers|June 22, 2023
Liquid Biopsy in Early-Stage Lung Cancer: Current and Future Clinical ApplicationsOlivia Vandekerckhove, Kristof Cuppens, Karin Pat, et al.
BMC Medical Genomics|December 21, 2018
Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disabilityAlena Zablotskaya, Hilde Van Esch, Kevin J Verstrepen, et al.
American Journal of Medical Genetics|October 12, 2002
Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndromeSuzanna G M Frints, Guy Froyen, Peter Marynen, et al.
Frontiers in Behavioral Neuroscience|July 29, 2015
Nxf7 deficiency impairs social exploration and spatio-cognitive abilities as well as hippocampal synaptic plasticity in miceZsuzsanna Callaerts-Vegh, Tariq Ahmed, Ben Vermaercke, et al.
Pageof 8