Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Shoukier

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

Pageof 1
Sort By:
European Archives of Psychiatry and Clinical Neuroscience|October 28, 2016
Polymorphism of the brain-derived neurotrophic factor and dynamics of the seizure threshold of electroconvulsive therapyC Stephani, M Shoukier, R Ahmed, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 19, 2012
[Hermansky-Pudlak syndrome]A Atili, J Lübke, M Shoukier, et al.
Clinical Genetics|March 4, 2008
Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasiaM Shoukier, U Teske, A Weise, et al.
Cytogenetic and Genome Research|October 12, 2012
A family with an inverted tandem duplication 5q22.1q23.2T Schmidt, I Bartels, T Liehr, et al.
Familial Cancer|December 14, 2011
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German familiesS M Schneegans, A Rosenberger, U Engel, et al.
Clinical Genetics|December 24, 2010
Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningiomaB Zirn, L Arning, I Bartels, et al.
European Journal of Neurology|May 25, 2010
Evaluating the effect of spastin splice mutations by quantitative allele-specific expression assayS Klimpe, A Zibat, U Zechner, et al.
Cytogenetic and Genome Research|October 19, 2013
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8T Schmidt, T Bierhals, F Kortüm, et al.
Prenatal Diagnosis|December 13, 2025
Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal CasesI Bedei, A Feresin, R Zemet, et al.
Clinical Genetics|January 31, 2012
Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?M Shoukier, N Klein, B Auber, et al.
Pageof 1

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

Sort By:
Pageof 1
European Archives of Psychiatry and Clinical Neuroscience|October 28, 2016
Polymorphism of the brain-derived neurotrophic factor and dynamics of the seizure threshold of electroconvulsive therapyC Stephani, M Shoukier, R Ahmed, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 19, 2012
[Hermansky-Pudlak syndrome]A Atili, J Lübke, M Shoukier, et al.
Clinical Genetics|March 4, 2008
Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasiaM Shoukier, U Teske, A Weise, et al.
Cytogenetic and Genome Research|October 12, 2012
A family with an inverted tandem duplication 5q22.1q23.2T Schmidt, I Bartels, T Liehr, et al.
Familial Cancer|December 14, 2011
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German familiesS M Schneegans, A Rosenberger, U Engel, et al.
Clinical Genetics|December 24, 2010
Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningiomaB Zirn, L Arning, I Bartels, et al.
European Journal of Neurology|May 25, 2010
Evaluating the effect of spastin splice mutations by quantitative allele-specific expression assayS Klimpe, A Zibat, U Zechner, et al.
Cytogenetic and Genome Research|October 19, 2013
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8T Schmidt, T Bierhals, F Kortüm, et al.
Prenatal Diagnosis|December 13, 2025
Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal CasesI Bedei, A Feresin, R Zemet, et al.
Clinical Genetics|January 31, 2012
Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?M Shoukier, N Klein, B Auber, et al.
Pageof 1