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Yosr Bouhlal

Showing results (1-10 of 15) with videos related to

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Handbook of Clinical Neurology|August 11, 2011
Ataxia with vitamin E deficiency and abetalipoproteinemiaFayçal Hentati, Ghada El-Euch, Yosr Bouhlal, et al.
Journal of Molecular Neuroscience : MN|June 17, 2009
A novel SACS gene mutation in a Tunisian familyYosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, et al.
Parkinsonism & Related Disorders|April 1, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overviewYosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, et al.
American Journal of Medical Genetics. Part A|May 3, 2013
Monoamniotic monochorionic twins discordant for noncompaction cardiomyopathyDianna Ng, Yosr Bouhlal, Philip C Ursell, et al.
Brain : a Journal of Neurology|December 27, 2013
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiencyGhada El Euch-Fayache, Yosr Bouhlal, Rim Amouri, et al.
Journal of Molecular Neuroscience : MN|July 28, 2009
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosisRim Amouri, Houda Nehdi, Yosr Bouhlal, et al.
Molecular Genetics & Genomic Medicine|September 17, 2013
Twin Mitochondrial Sequence AnalysisYosr Bouhlal, Selena Martinez, Henry Gong, et al.
Journal of Neurogenetics|June 24, 2008
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous familyYosr Bouhlal, Mourad Zouari, Mounir Kefi, et al.
Journal of Molecular Neuroscience : MN|March 19, 2011
Computational analysis of a novel SACS gene mutation with BioExtract serverYosr Bouhlal, Douglas M Jennewein, Brent Anderson, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 13, 2020
Integrated genomic characterization of ERBB2/HER2 alterations in invasive breast carcinoma: a focus on unusual FISH groupsSoo-Ryum Yang, Yosr Bouhlal, Francisco M De La Vega, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Handbook of Clinical Neurology|August 11, 2011
Ataxia with vitamin E deficiency and abetalipoproteinemiaFayçal Hentati, Ghada El-Euch, Yosr Bouhlal, et al.
Journal of Molecular Neuroscience : MN|June 17, 2009
A novel SACS gene mutation in a Tunisian familyYosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, et al.
Parkinsonism & Related Disorders|April 1, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overviewYosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, et al.
American Journal of Medical Genetics. Part A|May 3, 2013
Monoamniotic monochorionic twins discordant for noncompaction cardiomyopathyDianna Ng, Yosr Bouhlal, Philip C Ursell, et al.
Brain : a Journal of Neurology|December 27, 2013
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiencyGhada El Euch-Fayache, Yosr Bouhlal, Rim Amouri, et al.
Journal of Molecular Neuroscience : MN|July 28, 2009
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosisRim Amouri, Houda Nehdi, Yosr Bouhlal, et al.
Molecular Genetics & Genomic Medicine|September 17, 2013
Twin Mitochondrial Sequence AnalysisYosr Bouhlal, Selena Martinez, Henry Gong, et al.
Journal of Neurogenetics|June 24, 2008
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous familyYosr Bouhlal, Mourad Zouari, Mounir Kefi, et al.
Journal of Molecular Neuroscience : MN|March 19, 2011
Computational analysis of a novel SACS gene mutation with BioExtract serverYosr Bouhlal, Douglas M Jennewein, Brent Anderson, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 13, 2020
Integrated genomic characterization of ERBB2/HER2 alterations in invasive breast carcinoma: a focus on unusual FISH groupsSoo-Ryum Yang, Yosr Bouhlal, Francisco M De La Vega, et al.
Pageof 2