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

Mahmut S Sagiroglu

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Performance comparison of Next Generation sequencing platformsBekir Erguner, Duran Ustek, Mahmut S Sagiroglu
Clinical Dysmorphology|August 23, 2016
A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutationAli Dursun, Dilek Yalnizoglu, Omer F Gerdan, et al.
Epilepsy Research|May 20, 2015
A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous familyFeyza N Tuncer, Zeliha Gormez, Mustafa Calik, et al.
Human Molecular Genetics|July 12, 2015
Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesisAsuman Koparir, Omer F Karatas, Betul Yuceturk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2018
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndromePleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2019
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndromePleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Performance comparison of Next Generation sequencing platformsBekir Erguner, Duran Ustek, Mahmut S Sagiroglu
Clinical Dysmorphology|August 23, 2016
A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutationAli Dursun, Dilek Yalnizoglu, Omer F Gerdan, et al.
Epilepsy Research|May 20, 2015
A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous familyFeyza N Tuncer, Zeliha Gormez, Mustafa Calik, et al.
Human Molecular Genetics|July 12, 2015
Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesisAsuman Koparir, Omer F Karatas, Betul Yuceturk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2018
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndromePleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2019
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndromePleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Pageof 1