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 (121-130 of 235) with videos related to

Pageof 24
Sort By:
Annali Italiani Di Chirurgia|April 28, 2017
Protective effects of ursodeoxycholic acid in experimental corrosive esophagitis injury in ratsAdem Ku Çu K, Naci Topaloglu, Sule Yildirim, et al.
Urology|July 4, 2018
Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic FailureRaul I Clavijo, Himanshu Arora, Eric Gibbs, et al.
Colombia Medica (Cali, Colombia)|May 27, 2016
Do we really ponder about necessity of intravenous hydration in acute bronchiolitis?Şule Yıldırım, Nazan Kaymaz, Naci Topaloğlu, et al.
The Turkish Journal of Pediatrics|July 15, 2016
Prolonged pacifier usage in infancy does not cause eating behavior problem laterNazan Kaymaz, Şule Yıldırım, Sibel Cevizci, et al.
American Journal of Medical Genetics. Part A|February 13, 2024
EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorderIrman Forghani, Steven H Lang, Matthew J Rodier, et al.
Journal of Pediatric Genetics|May 13, 2017
Novel Causative Variants in <i>DYRK1A, KARS</i>, and <i>KAT6A</i> Associated with Intellectual Disability and Additional Phenotypic FeaturesClark R Murray, Samantha N Abel, Matthew B McClure, et al.
Molecular Genetics & Genomic Medicine|March 5, 2022
Genome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic diseaseNicholas Borja, Stephanie Bivona, Lé Shon Peart, et al.
Genetic Testing and Molecular Biomarkers|July 26, 2014
Identification of copy number variants through whole-exome sequencing in autosomal recessive nonsyndromic hearing lossGuney Bademci, Oscar Diaz-Horta, Shengru Guo, et al.
Human Genetics|June 9, 2019
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing lossClaire J Sineni, Muzeyyen Yildirim-Baylan, Shengru Guo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2007
Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 geneSerap Teber, Taner Sezer, Mehpare Kafali, et al.
Pageof 24

Showing results (121-130 of 235) with videos related to

Sort By:
Pageof 24
Annali Italiani Di Chirurgia|April 28, 2017
Protective effects of ursodeoxycholic acid in experimental corrosive esophagitis injury in ratsAdem Ku Çu K, Naci Topaloglu, Sule Yildirim, et al.
Urology|July 4, 2018
Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic FailureRaul I Clavijo, Himanshu Arora, Eric Gibbs, et al.
Colombia Medica (Cali, Colombia)|May 27, 2016
Do we really ponder about necessity of intravenous hydration in acute bronchiolitis?Şule Yıldırım, Nazan Kaymaz, Naci Topaloğlu, et al.
The Turkish Journal of Pediatrics|July 15, 2016
Prolonged pacifier usage in infancy does not cause eating behavior problem laterNazan Kaymaz, Şule Yıldırım, Sibel Cevizci, et al.
American Journal of Medical Genetics. Part A|February 13, 2024
EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorderIrman Forghani, Steven H Lang, Matthew J Rodier, et al.
Journal of Pediatric Genetics|May 13, 2017
Novel Causative Variants in <i>DYRK1A, KARS</i>, and <i>KAT6A</i> Associated with Intellectual Disability and Additional Phenotypic FeaturesClark R Murray, Samantha N Abel, Matthew B McClure, et al.
Molecular Genetics & Genomic Medicine|March 5, 2022
Genome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic diseaseNicholas Borja, Stephanie Bivona, Lé Shon Peart, et al.
Genetic Testing and Molecular Biomarkers|July 26, 2014
Identification of copy number variants through whole-exome sequencing in autosomal recessive nonsyndromic hearing lossGuney Bademci, Oscar Diaz-Horta, Shengru Guo, et al.
Human Genetics|June 9, 2019
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing lossClaire J Sineni, Muzeyyen Yildirim-Baylan, Shengru Guo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2007
Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 geneSerap Teber, Taner Sezer, Mehpare Kafali, et al.
Pageof 24