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Wim Wuyts

Showing results (61-70 of 135) with videos related to

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American Journal of Medical Genetics. Part A|February 26, 2005
An interstitial deletion of chromosome 7 at band q21: a case report and reviewWinnie Courtens, Stefan Vermeulen, Wim Wuyts, et al.
Human Mutation|June 29, 2004
Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostosesStefan J White, Geraldine R Vink, Marjolein Kriek, et al.
Gene|November 1, 2011
Identification and functional characterization of the human EXT1 promoter regionIvy Jennes, Monia Zuntini, Kirsten Mees, et al.
Chest|August 16, 2025
Mortality Outcomes and ACE Inhibitor Use in Patients with Idiopathic Pulmonary FibrosisBurcu Ozaltin, Robert Chapman, Tine Follet, et al.
Genes|April 30, 2021
A New Pathogenic Variant in <i>POU3F4</i> Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative SurgeryAhmet M Tekin, Marco Matulic, Wim Wuyts, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
Carnitine-palmitoyltransferase 2 deficiency: novel mutations and relevance of newborn screeningSabine Illsinger, Thomas Lücke, Michael Peter, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 22, 2023
Targeted Next-Generation Sequencing in Children With Bilateral Sensorineural Hearing Loss: Diagnostic Yield and Predictors of a Genetic CauseAn Boudewyns, Jenneke van den Ende, Nils Peeters, et al.
European Journal of Human Genetics : EJHG|February 17, 2018
Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairmentSebastien P F JanssensdeVarebeke, Guy Van Camp, Nils Peeters, et al.
Mitochondrion|September 16, 2008
Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patientsAnnelies Konings, Guy Van Camp, Alain Goethals, et al.
Respiration; International Review of Thoracic Diseases|April 12, 2017
Antacid Therapy and Disease Progression in Patients with Idiopathic Pulmonary Fibrosis Who Received PirfenidoneMichael Kreuter, Paolo Spagnolo, Wim Wuyts, et al.
Pageof 14

Showing results (61-70 of 135) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|February 26, 2005
An interstitial deletion of chromosome 7 at band q21: a case report and reviewWinnie Courtens, Stefan Vermeulen, Wim Wuyts, et al.
Human Mutation|June 29, 2004
Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostosesStefan J White, Geraldine R Vink, Marjolein Kriek, et al.
Gene|November 1, 2011
Identification and functional characterization of the human EXT1 promoter regionIvy Jennes, Monia Zuntini, Kirsten Mees, et al.
Chest|August 16, 2025
Mortality Outcomes and ACE Inhibitor Use in Patients with Idiopathic Pulmonary FibrosisBurcu Ozaltin, Robert Chapman, Tine Follet, et al.
Genes|April 30, 2021
A New Pathogenic Variant in <i>POU3F4</i> Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative SurgeryAhmet M Tekin, Marco Matulic, Wim Wuyts, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
Carnitine-palmitoyltransferase 2 deficiency: novel mutations and relevance of newborn screeningSabine Illsinger, Thomas Lücke, Michael Peter, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 22, 2023
Targeted Next-Generation Sequencing in Children With Bilateral Sensorineural Hearing Loss: Diagnostic Yield and Predictors of a Genetic CauseAn Boudewyns, Jenneke van den Ende, Nils Peeters, et al.
European Journal of Human Genetics : EJHG|February 17, 2018
Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairmentSebastien P F JanssensdeVarebeke, Guy Van Camp, Nils Peeters, et al.
Mitochondrion|September 16, 2008
Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patientsAnnelies Konings, Guy Van Camp, Alain Goethals, et al.
Respiration; International Review of Thoracic Diseases|April 12, 2017
Antacid Therapy and Disease Progression in Patients with Idiopathic Pulmonary Fibrosis Who Received PirfenidoneMichael Kreuter, Paolo Spagnolo, Wim Wuyts, et al.
Pageof 14