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Guy Froyen

Showing results (21-30 of 77) with videos related to

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Biopreservation and Biobanking|November 10, 2018
Archival May-Grünwald-Giemsa-Stained Bone Marrow Smears Are an Eligible Source for Molecular DNA ResearchBénedith Oben, Charlotte Cosemans, Ingrid Arijs, et al.
Clinical Lymphoma, Myeloma & Leukemia|March 7, 2018
Prognostic Biomarkers in the Progression From MGUS to Multiple Myeloma: A Systematic ReviewCharlotte Cosemans, Bénedith Oben, Ingrid Arijs, et al.
Prenatal Diagnosis|November 5, 2011
A longer tracheal occlusion period results in increased lung growth in the nitrofen rat modelVeronika Beck, Marcus G Davey, Steffi Mayer, et al.
Microbiology (Reading, England)|March 9, 2000
Single allele knock-out of Candida albicans CGT1 leads to unexpected resistance to hygromycin B and elevated temperatureMarianne D De Backer, Ronald A de Hoogt, Guy Froyen, et al.
Human Genetics|July 20, 2014
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivationNathalie Fieremans, Marijke Bauters, Stefanie Belet, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
PAK3 related mental disability: further characterization of the phenotypeMaarit Peippo, Anne M Koivisto, Teppo Särkämö, et al.
Human Mutation|June 5, 2007
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genesGuy Froyen, Hilde Van Esch, Marijke Bauters, et al.
Plos One|May 16, 2013
Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disabilityLieselot Vanmarsenille, Jelle Verbeeck, Stefanie Belet, et al.
Human Molecular Genetics|May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosisHilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.
Pediatrics|September 21, 2011
A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3María-Isabel Tejada, Cristina Martínez-Bouzas, Ainhoa García-Ribes, et al.
Pageof 8

Showing results (21-30 of 77) with videos related to

Sort By:
Pageof 8
Biopreservation and Biobanking|November 10, 2018
Archival May-Grünwald-Giemsa-Stained Bone Marrow Smears Are an Eligible Source for Molecular DNA ResearchBénedith Oben, Charlotte Cosemans, Ingrid Arijs, et al.
Clinical Lymphoma, Myeloma & Leukemia|March 7, 2018
Prognostic Biomarkers in the Progression From MGUS to Multiple Myeloma: A Systematic ReviewCharlotte Cosemans, Bénedith Oben, Ingrid Arijs, et al.
Prenatal Diagnosis|November 5, 2011
A longer tracheal occlusion period results in increased lung growth in the nitrofen rat modelVeronika Beck, Marcus G Davey, Steffi Mayer, et al.
Microbiology (Reading, England)|March 9, 2000
Single allele knock-out of Candida albicans CGT1 leads to unexpected resistance to hygromycin B and elevated temperatureMarianne D De Backer, Ronald A de Hoogt, Guy Froyen, et al.
Human Genetics|July 20, 2014
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivationNathalie Fieremans, Marijke Bauters, Stefanie Belet, et al.
American Journal of Medical Genetics. Part A|September 14, 2007
PAK3 related mental disability: further characterization of the phenotypeMaarit Peippo, Anne M Koivisto, Teppo Särkämö, et al.
Human Mutation|June 5, 2007
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genesGuy Froyen, Hilde Van Esch, Marijke Bauters, et al.
Plos One|May 16, 2013
Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disabilityLieselot Vanmarsenille, Jelle Verbeeck, Stefanie Belet, et al.
Human Molecular Genetics|May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosisHilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.
Pediatrics|September 21, 2011
A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3María-Isabel Tejada, Cristina Martínez-Bouzas, Ainhoa García-Ribes, et al.
Pageof 8