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

Mustafa Tekin

Showing results (101-110 of 235) with videos related to

Pageof 24
Sort By:
International Journal of Pediatric Otorhinolaryngology|September 14, 2016
Audiological findings in Noonan syndromeSuna Tokgoz-Yilmaz, Meral Didem Turkyilmaz, Filiz Basak Cengiz, et al.
Scientific Reports|October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing lossMemoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Clinical Case Reports|April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutationIbis Menendez, Claudia Carranza, Mariana Herrera, et al.
Arthritis and Rheumatism|May 14, 2013
DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndromeZ Birsin Ozçakar, Joseph Foster, Oscar Diaz-Horta, et al.
Human Genetics|April 10, 2002
Molecular characterization of a ring X chromosome in a male with short statureJay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|June 24, 2015
Serum Ischemia-Modified Albumin Levels in Experimental Model of Acute PancreatitisNaci Topaloglu, Adem Kucuk, Mustafa Tekin, et al.
Fertility and Sterility|June 21, 2011
Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndromeKemal O Yariz, Tom Walsh, Asli Uzak, et al.
Anatomical Record (Hoboken, N.J. : 2007)|July 2, 2019
The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 SystemBing Zou, Alexandra A Desmidt, Rahul Mittal, et al.
Clinical Genetics|July 19, 2002
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish familyMustafa Tekin, F Doğu, N Taçyíldiz, et al.
Hearing Research|February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genesDemet Tekin, Denise Yan, Guney Bademci, et al.
Pageof 24

Showing results (101-110 of 235) with videos related to

Sort By:
Pageof 24
International Journal of Pediatric Otorhinolaryngology|September 14, 2016
Audiological findings in Noonan syndromeSuna Tokgoz-Yilmaz, Meral Didem Turkyilmaz, Filiz Basak Cengiz, et al.
Scientific Reports|October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing lossMemoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Clinical Case Reports|April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutationIbis Menendez, Claudia Carranza, Mariana Herrera, et al.
Arthritis and Rheumatism|May 14, 2013
DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndromeZ Birsin Ozçakar, Joseph Foster, Oscar Diaz-Horta, et al.
Human Genetics|April 10, 2002
Molecular characterization of a ring X chromosome in a male with short statureJay W Ellison, Mustafa Tekin, Karen Salvasen Sikes, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|June 24, 2015
Serum Ischemia-Modified Albumin Levels in Experimental Model of Acute PancreatitisNaci Topaloglu, Adem Kucuk, Mustafa Tekin, et al.
Fertility and Sterility|June 21, 2011
Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndromeKemal O Yariz, Tom Walsh, Asli Uzak, et al.
Anatomical Record (Hoboken, N.J. : 2007)|July 2, 2019
The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 SystemBing Zou, Alexandra A Desmidt, Rahul Mittal, et al.
Clinical Genetics|July 19, 2002
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish familyMustafa Tekin, F Doğu, N Taçyíldiz, et al.
Hearing Research|February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genesDemet Tekin, Denise Yan, Guney Bademci, et al.
Pageof 24