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Wim Wuyts

Showing results (51-60 of 135) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 12, 2018
Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf ChildrenAn Boudewyns, Jenneke van den Ende, Manou Sommen, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defectsKatie M G Snape, Deborah Ruddy, Martin Zenker, et al.
The International Journal of Cardiovascular Imaging|August 23, 2014
Prediction of hemodynamic improvement after pulmonary endarterectomy in chronic thromboembolic pulmonary hypertension using non-invasive imagingBastiaan E Schölzel, Martijn C Post, Alexander van de Bruaene, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 14, 2020
Etiological Work-up in Referrals From Neonatal Hearing Screening: 20 Years of ExperienceAn Boudewyns, Jenneke van den Ende, Frank Declau, et al.
Human Mutation|February 1, 2011
Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patientsKároly Szuhai, Ivy Jennes, Danielle de Jong, et al.
Bioinformatics (Oxford, England)|November 28, 2022
varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS dataAjay Anand Kumar, Bart Loeys, Gerarda Van De Beek, et al.
Human Mutation|October 8, 2009
Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)Ivy Jennes, Elena Pedrini, Monia Zuntini, et al.
Heart (British Cardiac Society)|February 18, 2015
Exercise pathophysiology and sildenafil effects in chronic thromboembolic pulmonary hypertensionGuido Claessen, Andre La Gerche, Jean-Yves Wielandts, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and reviewWinnie Courtens, Wim Wuyts, Martin Poot, et al.
The Journal of Molecular Diagnostics : JMD|February 9, 2008
Detection of microsatellite instability in colorectal cancer using an alternative multiplex assay of quasi-monomorphic mononucleotide markersVanessa Deschoolmeester, Marc Baay, Wim Wuyts, et al.
Pageof 14

Showing results (51-60 of 135) with videos related to

Sort By:
Pageof 14
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 12, 2018
Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf ChildrenAn Boudewyns, Jenneke van den Ende, Manou Sommen, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defectsKatie M G Snape, Deborah Ruddy, Martin Zenker, et al.
The International Journal of Cardiovascular Imaging|August 23, 2014
Prediction of hemodynamic improvement after pulmonary endarterectomy in chronic thromboembolic pulmonary hypertension using non-invasive imagingBastiaan E Schölzel, Martijn C Post, Alexander van de Bruaene, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 14, 2020
Etiological Work-up in Referrals From Neonatal Hearing Screening: 20 Years of ExperienceAn Boudewyns, Jenneke van den Ende, Frank Declau, et al.
Human Mutation|February 1, 2011
Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patientsKároly Szuhai, Ivy Jennes, Danielle de Jong, et al.
Bioinformatics (Oxford, England)|November 28, 2022
varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS dataAjay Anand Kumar, Bart Loeys, Gerarda Van De Beek, et al.
Human Mutation|October 8, 2009
Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)Ivy Jennes, Elena Pedrini, Monia Zuntini, et al.
Heart (British Cardiac Society)|February 18, 2015
Exercise pathophysiology and sildenafil effects in chronic thromboembolic pulmonary hypertensionGuido Claessen, Andre La Gerche, Jean-Yves Wielandts, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and reviewWinnie Courtens, Wim Wuyts, Martin Poot, et al.
The Journal of Molecular Diagnostics : JMD|February 9, 2008
Detection of microsatellite instability in colorectal cancer using an alternative multiplex assay of quasi-monomorphic mononucleotide markersVanessa Deschoolmeester, Marc Baay, Wim Wuyts, et al.
Pageof 14