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 (141-150 of 235) with videos related to

Pageof 24
Sort By:
Human Mutation|March 7, 2013
GEnomes Management Application (GEM.app): a new software tool for large-scale collaborative genome analysisMichael A Gonzalez, Rafael F Acosta Lebrigio, Derek Van Booven, et al.
Ophthalmic Genetics|March 4, 2020
X-linked peripheral retinoschisis without macular involvement: a case series with <i>RS1</i> genetic confirmationLogan M Smith, Linda A Cernichiaro-Espinosa, Craig A McKeown, et al.
Biochemical Genetics|January 9, 2026
Spectrum of DNA Variants Underlying Deafness in an Ecuadorian CohortAnghela Reinoso-Castillo, Memoona Ramzan, Andrea Carrera-Gonzalez, et al.
American Journal of Ophthalmology Case Reports|August 22, 2019
A unique case of vision loss in a patient with hypotrichosis and juvenile macular dystrophy and primary ciliary dyskinesiaKenneth C Fan, Nimesh A Patel, Nicolas A Yannuzzi, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 9, 2015
Effect of delivery mode on postpartum neonatal body temperaturesNaci Topaloğlu, Fatih Köksal Binnetoğlu, Şule Yıldırım, et al.
Annals of Human Genetics|March 6, 2010
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deafMustafa Tekin, Xia-Juan Xia, Radnaabazar Erdenetungalag, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 9, 2014
Complement activation by ligand-driven juxtaposition of discrete pattern recognition complexesSøren E Degn, Troels R Kjaer, Rune T Kidmose, et al.
Journal of Inherited Metabolic Disease|August 5, 2020
A founder noncoding GALT variant interfering with splicing causes galactosemiaKumarie Latchman, Jeanette Brown, Claire J Sineni, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 10, 2020
Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2Christine T Dinh, Eric Nisenbaum, Darius Chyou, et al.
Human Genetics|April 10, 2002
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephalyJeffrey E Ming, Michelle E Kaupas, Erich Roessler, et al.
Pageof 24

Showing results (141-150 of 235) with videos related to

Sort By:
Pageof 24
Human Mutation|March 7, 2013
GEnomes Management Application (GEM.app): a new software tool for large-scale collaborative genome analysisMichael A Gonzalez, Rafael F Acosta Lebrigio, Derek Van Booven, et al.
Ophthalmic Genetics|March 4, 2020
X-linked peripheral retinoschisis without macular involvement: a case series with <i>RS1</i> genetic confirmationLogan M Smith, Linda A Cernichiaro-Espinosa, Craig A McKeown, et al.
Biochemical Genetics|January 9, 2026
Spectrum of DNA Variants Underlying Deafness in an Ecuadorian CohortAnghela Reinoso-Castillo, Memoona Ramzan, Andrea Carrera-Gonzalez, et al.
American Journal of Ophthalmology Case Reports|August 22, 2019
A unique case of vision loss in a patient with hypotrichosis and juvenile macular dystrophy and primary ciliary dyskinesiaKenneth C Fan, Nimesh A Patel, Nicolas A Yannuzzi, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 9, 2015
Effect of delivery mode on postpartum neonatal body temperaturesNaci Topaloğlu, Fatih Köksal Binnetoğlu, Şule Yıldırım, et al.
Annals of Human Genetics|March 6, 2010
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deafMustafa Tekin, Xia-Juan Xia, Radnaabazar Erdenetungalag, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 9, 2014
Complement activation by ligand-driven juxtaposition of discrete pattern recognition complexesSøren E Degn, Troels R Kjaer, Rune T Kidmose, et al.
Journal of Inherited Metabolic Disease|August 5, 2020
A founder noncoding GALT variant interfering with splicing causes galactosemiaKumarie Latchman, Jeanette Brown, Claire J Sineni, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 10, 2020
Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2Christine T Dinh, Eric Nisenbaum, Darius Chyou, et al.
Human Genetics|April 10, 2002
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephalyJeffrey E Ming, Michelle E Kaupas, Erich Roessler, et al.
Pageof 24