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Froyen

Showing results (111-120 of 172) with videos related to

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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.
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.
American Journal of Medical Genetics. Part A|November 12, 2005
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndromeFernanda Sarquis Jehee, Carla Rosenberg, Ana Cristina Krepischi-Santos, et al.
The Lancet. Psychiatry|August 27, 2019
Belgian Superior Health Council advises against the use of the DSM categoriesStijn Vanheule, Pieter Adriaens, Ariane Bazan, et al.
International Journal of Pharmaceutics|July 13, 2010
Potential of amorphous microporous silica for ibuprofen controlled releaseC A Aerts, E Verraedt, A Depla, et al.
The Lancet. Psychiatry|October 22, 2019
Points to consider regarding DSM alternatives - Authors' replyStijn Vanheule, Pieter Adriaens, Ariane Bazan, et al.
Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.
European Journal of Human Genetics : EJHG|June 21, 2007
Partial duplications of the ATRX gene cause the ATR-X syndromeBernard Thienpont, Thomy de Ravel, Hilde Van Esch, et al.
Cancers|February 25, 2022
The Dynamics of Nucleotide Variants in the Progression from Low-Intermediate Myeloma Precursor Conditions to Multiple Myeloma: Studying Serial Samples with a Targeted Sequencing ApproachBénedith Oben, Charlotte Cosemans, Ellen Geerdens, et al.
Pageof 18

Showing results (111-120 of 172) with videos related to

Sort By:
Pageof 18
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.
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.
American Journal of Medical Genetics. Part A|November 12, 2005
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndromeFernanda Sarquis Jehee, Carla Rosenberg, Ana Cristina Krepischi-Santos, et al.
The Lancet. Psychiatry|August 27, 2019
Belgian Superior Health Council advises against the use of the DSM categoriesStijn Vanheule, Pieter Adriaens, Ariane Bazan, et al.
International Journal of Pharmaceutics|July 13, 2010
Potential of amorphous microporous silica for ibuprofen controlled releaseC A Aerts, E Verraedt, A Depla, et al.
The Lancet. Psychiatry|October 22, 2019
Points to consider regarding DSM alternatives - Authors' replyStijn Vanheule, Pieter Adriaens, Ariane Bazan, et al.
Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.
European Journal of Human Genetics : EJHG|June 21, 2007
Partial duplications of the ATRX gene cause the ATR-X syndromeBernard Thienpont, Thomy de Ravel, Hilde Van Esch, et al.
Cancers|February 25, 2022
The Dynamics of Nucleotide Variants in the Progression from Low-Intermediate Myeloma Precursor Conditions to Multiple Myeloma: Studying Serial Samples with a Targeted Sequencing ApproachBénedith Oben, Charlotte Cosemans, Ellen Geerdens, et al.
Pageof 18