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Yavuz Sahin

Showing results (1-10 of 23) with videos related to

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Environmental Monitoring and Assessment|May 17, 2023
3D modelling of surface spreading and underground dam groundwater recharge: Egri Creek Subbasin, TurkeyYavuz Sahin, Gokmen Tayfur
Environmental Monitoring and Assessment|August 28, 2023
Correction to: 3D modelling of surface spreading and underground dam groundwater recharge: Egri Creek Subbasin, TurkeyYavuz Sahin, Gokmen Tayfur
Ophthalmic Genetics|September 12, 2022
Seroreactivity against retinal proteins in a case of POC1B gene associated cone dystrophy with normal funduscopic appearance: a systematic approach to diagnosisÖzge Yanık, Figen Batıoğlu, Yavuz Sahin, et al.
Indian Journal of Ophthalmology|July 6, 2022
The genetic counseling in a patient affected by choroideremia solved with the whole-exome sequencing approachBedia Sahin, Erik Burton, Okkes Kuybu, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Interstitial deletion 5p14.1-p15.2 and 5q14.3-q23.2 in a patient with clubfoot, blepharophimosis, arthrogryposis, and multiple congenital abnormalitiesBurhan Balta, Murat Erdogan, Ayse B Ergul, et al.
Pediatric Dermatology|April 28, 2025
Poikiloderma With Neutropenia due to Novel USB1 MutationKerem Balan, Basak Yalici-Armagan, Neslihan Akdogan, et al.
Brain & Development|September 20, 2016
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresisYavuz Sahin, Olcay Güngör, Akif Ayaz, et al.
Acta Neurologica Belgica|November 16, 2016
Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsyYavuz Sahin, Olcay Güngör, Zeliha Gormez, et al.
Molecular Syndromology|April 8, 2024
A Homozygous Missense Variant in <i>HSD17B4</i> Identified in Two Different FamiliesPınar Özkan Kart, Yavuz Sahin, Nihal Yildiz, et al.
Clinical Dysmorphology|October 21, 2016
The TWIST2 mutation causes Setleis syndrome: a rare clinical case reportAkif Ayaz, Sinem Yalcintepe, Ozge Ozalp Yuregir, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Environmental Monitoring and Assessment|May 17, 2023
3D modelling of surface spreading and underground dam groundwater recharge: Egri Creek Subbasin, TurkeyYavuz Sahin, Gokmen Tayfur
Environmental Monitoring and Assessment|August 28, 2023
Correction to: 3D modelling of surface spreading and underground dam groundwater recharge: Egri Creek Subbasin, TurkeyYavuz Sahin, Gokmen Tayfur
Ophthalmic Genetics|September 12, 2022
Seroreactivity against retinal proteins in a case of POC1B gene associated cone dystrophy with normal funduscopic appearance: a systematic approach to diagnosisÖzge Yanık, Figen Batıoğlu, Yavuz Sahin, et al.
Indian Journal of Ophthalmology|July 6, 2022
The genetic counseling in a patient affected by choroideremia solved with the whole-exome sequencing approachBedia Sahin, Erik Burton, Okkes Kuybu, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Interstitial deletion 5p14.1-p15.2 and 5q14.3-q23.2 in a patient with clubfoot, blepharophimosis, arthrogryposis, and multiple congenital abnormalitiesBurhan Balta, Murat Erdogan, Ayse B Ergul, et al.
Pediatric Dermatology|April 28, 2025
Poikiloderma With Neutropenia due to Novel USB1 MutationKerem Balan, Basak Yalici-Armagan, Neslihan Akdogan, et al.
Brain & Development|September 20, 2016
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresisYavuz Sahin, Olcay Güngör, Akif Ayaz, et al.
Acta Neurologica Belgica|November 16, 2016
Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsyYavuz Sahin, Olcay Güngör, Zeliha Gormez, et al.
Molecular Syndromology|April 8, 2024
A Homozygous Missense Variant in <i>HSD17B4</i> Identified in Two Different FamiliesPınar Özkan Kart, Yavuz Sahin, Nihal Yildiz, et al.
Clinical Dysmorphology|October 21, 2016
The TWIST2 mutation causes Setleis syndrome: a rare clinical case reportAkif Ayaz, Sinem Yalcintepe, Ozge Ozalp Yuregir, et al.
Pageof 3