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B Cengiz

Showing results (61-70 of 68) with videos related to

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Archivos Argentinos De Pediatria|November 24, 2015
[Pediatric-onset adult type sarcoidosis: A case report]Yasemin Ozsurekci, Ali B Cengiz, Ali Duzova, et al.
Genes|April 1, 2020
Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South FloridaSaradadevi Thanikachalam, Elizabeth Hodapp, Ta C Chang, et al.
Clinical Genetics|April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontiaM Tekin, H Oztürkmen Akay, S Fitoz, et al.
The Journal of Clinical Investigation|May 6, 2020
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear developmentGuney Bademci, Clemer Abad, Filiz B Cengiz, et al.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Scientific Reports|August 27, 2016
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossG Bademci, F B Cengiz, J Foster Ii, et al.
Human Genetics|July 9, 2018
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing lossGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 26, 2023
Estimating motor unit numbers from a CMAP scan: Repeatability study on three muscles at 15 centresD M Sørensen, H Bostock, A Abrahao, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Archivos Argentinos De Pediatria|November 24, 2015
[Pediatric-onset adult type sarcoidosis: A case report]Yasemin Ozsurekci, Ali B Cengiz, Ali Duzova, et al.
Genes|April 1, 2020
Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South FloridaSaradadevi Thanikachalam, Elizabeth Hodapp, Ta C Chang, et al.
Clinical Genetics|April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontiaM Tekin, H Oztürkmen Akay, S Fitoz, et al.
The Journal of Clinical Investigation|May 6, 2020
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear developmentGuney Bademci, Clemer Abad, Filiz B Cengiz, et al.
Human Molecular Genetics|December 19, 2018
FOXF2 is required for cochlear development in humans and miceGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Scientific Reports|August 27, 2016
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossG Bademci, F B Cengiz, J Foster Ii, et al.
Human Genetics|July 9, 2018
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing lossGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 26, 2023
Estimating motor unit numbers from a CMAP scan: Repeatability study on three muscles at 15 centresD M Sørensen, H Bostock, A Abrahao, et al.
Pageof 7