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Figen Seymen

Showing results (41-50 of 82) with videos related to

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European Journal of Oral Sciences|May 6, 2006
Mutational analysis of candidate genes in 24 amelogenesis imperfecta familiesJung-Wook Kim, James P Simmer, Brent P-L Lin, et al.
Oral Diseases|November 3, 2022
Phenotypic variability in LAMA3-associated amelogenesis imperfectaShih-Kai Wang, Hong Zhang, Yin-Lin Wang, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|December 3, 2014
Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutationCurtis R Herzog, Bryan M Reid, Figen Seymen, et al.
Nephron|February 14, 2018
Nephrocalcinosis in Amelogenesis Imperfecta Caused by the FAM20A MutationMine Koruyucu, Figen Seymen, Genco Gencay, et al.
Oral Diseases|May 24, 2021
Novel homozygous KREMEN1 mutation causes ectodermal dysplasiaYejin Lee, Hong Zhang, Figen Seymen, et al.
Journal of Personalized Medicine|February 25, 2023
Novel <i>WDR72</i> Mutations Causing Hypomaturation Amelogenesis ImperfectaYoun Jung Kim, Hong Zhang, Yejin Lee, et al.
Journal of Personalized Medicine|February 25, 2022
Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis ImperfectaYejin Lee, Hong Zhang, Figen Seymen, et al.
International Journal of Molecular Sciences|June 19, 2024
<i>AMELX</i> Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis ImperfectaShih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Clinical Oral Investigations|March 10, 2016
Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glandsFigen Seymen, Mine Koruyucu, Ismet Rezani Toptanci, et al.
European Journal of Dentistry|September 15, 2020
Investigating the Level of Knowledge of the Community about Oral and Dental HealthSinem Birant, Mine Koruyucu, Hazal Ozcan, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
European Journal of Oral Sciences|May 6, 2006
Mutational analysis of candidate genes in 24 amelogenesis imperfecta familiesJung-Wook Kim, James P Simmer, Brent P-L Lin, et al.
Oral Diseases|November 3, 2022
Phenotypic variability in LAMA3-associated amelogenesis imperfectaShih-Kai Wang, Hong Zhang, Yin-Lin Wang, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|December 3, 2014
Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutationCurtis R Herzog, Bryan M Reid, Figen Seymen, et al.
Nephron|February 14, 2018
Nephrocalcinosis in Amelogenesis Imperfecta Caused by the FAM20A MutationMine Koruyucu, Figen Seymen, Genco Gencay, et al.
Oral Diseases|May 24, 2021
Novel homozygous KREMEN1 mutation causes ectodermal dysplasiaYejin Lee, Hong Zhang, Figen Seymen, et al.
Journal of Personalized Medicine|February 25, 2023
Novel <i>WDR72</i> Mutations Causing Hypomaturation Amelogenesis ImperfectaYoun Jung Kim, Hong Zhang, Yejin Lee, et al.
Journal of Personalized Medicine|February 25, 2022
Novel <i>KLK4</i> Mutations Cause Hypomaturation Amelogenesis ImperfectaYejin Lee, Hong Zhang, Figen Seymen, et al.
International Journal of Molecular Sciences|June 19, 2024
<i>AMELX</i> Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis ImperfectaShih-Kai Wang, Hong Zhang, Hua-Chieh Lin, et al.
Clinical Oral Investigations|March 10, 2016
Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glandsFigen Seymen, Mine Koruyucu, Ismet Rezani Toptanci, et al.
European Journal of Dentistry|September 15, 2020
Investigating the Level of Knowledge of the Community about Oral and Dental HealthSinem Birant, Mine Koruyucu, Hazal Ozcan, et al.
Pageof 9