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 (21-30 of 235) with videos related to

Pageof 24
Sort By:
Molecular Cytogenetics|April 11, 2012
Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?Deling Li, Mustafa Tekin, Maria Buch, et al.
Molecular Biosystems|April 13, 2016
Next generation sequencing: implications in personalized medicine and pharmacogenomicsBahareh Rabbani, Hirofumi Nakaoka, Shahin Akhondzadeh, et al.
Journal of Nephrology|July 29, 2006
Serum amyloid A1 -13 T/C alleles in Turkish familial Mediterranean fever patients with and without amyloidosisNejat Akar, Metis Hasipek, Ayşenur Oztürk, et al.
International Journal of Pediatric Otorhinolaryngology|May 23, 2006
Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypesBurcu Oztürk Hişmi, Suna Tokgöz Yilmaz, Armağan Incesulu, et al.
Human Biology|January 6, 2006
657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish populationMustafa Tekin, Duygu Akcayoz, Canan Ucar, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 21, 2013
Screening of families of patients with left-sided cardiovascular anomaliesFikri Demir, Cem Karadeniz, Semra Atalay, et al.
Case Reports in Emergency Medicine|June 14, 2013
Nontraumatic massive spontaneous hemothorax with concomitant warfarin useNurettin Özgür Doğan, Gül Pamukçu Günaydın, Mustafa Tekin, et al.
Genetic Testing and Molecular Biomarkers|June 7, 2013
Next-generation sequencing in genetic hearing lossDenise Yan, Mustafa Tekin, Susan H Blanton, et al.
Plos One|February 25, 2012
Challenges in whole exome sequencing: an example from hereditary deafnessAsli Sirmaci, Yvonne J K Edwards, Hatice Akay, et al.
International Journal of Pediatric Otorhinolaryngology|December 6, 2005
Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalitiesMustafa Tekin, Suat Fitoz, Serap Arici, et al.
Pageof 24

Showing results (21-30 of 235) with videos related to

Sort By:
Pageof 24
Molecular Cytogenetics|April 11, 2012
Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?Deling Li, Mustafa Tekin, Maria Buch, et al.
Molecular Biosystems|April 13, 2016
Next generation sequencing: implications in personalized medicine and pharmacogenomicsBahareh Rabbani, Hirofumi Nakaoka, Shahin Akhondzadeh, et al.
Journal of Nephrology|July 29, 2006
Serum amyloid A1 -13 T/C alleles in Turkish familial Mediterranean fever patients with and without amyloidosisNejat Akar, Metis Hasipek, Ayşenur Oztürk, et al.
International Journal of Pediatric Otorhinolaryngology|May 23, 2006
Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypesBurcu Oztürk Hişmi, Suna Tokgöz Yilmaz, Armağan Incesulu, et al.
Human Biology|January 6, 2006
657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish populationMustafa Tekin, Duygu Akcayoz, Canan Ucar, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 21, 2013
Screening of families of patients with left-sided cardiovascular anomaliesFikri Demir, Cem Karadeniz, Semra Atalay, et al.
Case Reports in Emergency Medicine|June 14, 2013
Nontraumatic massive spontaneous hemothorax with concomitant warfarin useNurettin Özgür Doğan, Gül Pamukçu Günaydın, Mustafa Tekin, et al.
Genetic Testing and Molecular Biomarkers|June 7, 2013
Next-generation sequencing in genetic hearing lossDenise Yan, Mustafa Tekin, Susan H Blanton, et al.
Plos One|February 25, 2012
Challenges in whole exome sequencing: an example from hereditary deafnessAsli Sirmaci, Yvonne J K Edwards, Hatice Akay, et al.
International Journal of Pediatric Otorhinolaryngology|December 6, 2005
Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalitiesMustafa Tekin, Suat Fitoz, Serap Arici, et al.
Pageof 24