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Figen Seymen

Showing results (61-70 of 82) with videos related to

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Clinical Oral Investigations|August 19, 2018
Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfectaYoun Jung Kim, Figen Seymen, Jenny Kang, et al.
International Journal of Oral Science|November 13, 2021
Correction: Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.
International Journal of Oral Science|October 1, 2021
Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
Fam83h null mice support a neomorphic mechanism for human ADHCAIShih-Kai Wang, Yuanyuan Hu, Jie Yang, et al.
Clinical Genetics|December 4, 2018
Mutations in RELT cause autosomal recessive amelogenesis imperfectaJung-Wook Kim, Hong Zhang, Figen Seymen, et al.
Archives of Oral Biology|June 25, 2013
Genes expressed in dental enamel development are associated with molar-incisor hypomineralizationFabiano Jeremias, Mine Koruyucu, Erika C Küchler, et al.
Oral Diseases|August 28, 2019
Novel frameshift mutations in DSPP cause dentin dysplasia type IIJi Won Lee, Jiwon Hong, Figen Seymen, et al.
European Journal of Oral Sciences|August 19, 2015
Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitionsMerve Bayram, Kathleen Deeley, Maria F Reis, et al.
Molecular Genetics & Genomic Medicine|June 5, 2020
Dental malformations associated with biallelic MMP20 mutationsShih-Kai Wang, Hong Zhang, Michael B Chavez, et al.
Genes|May 28, 2022
The Modified Shields Classification and 12 Families with Defined <i>DSPP</i> MutationsJames P Simmer, Hong Zhang, Sophie J H Moon, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Clinical Oral Investigations|August 19, 2018
Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfectaYoun Jung Kim, Figen Seymen, Jenny Kang, et al.
International Journal of Oral Science|November 13, 2021
Correction: Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.
International Journal of Oral Science|October 1, 2021
Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
Fam83h null mice support a neomorphic mechanism for human ADHCAIShih-Kai Wang, Yuanyuan Hu, Jie Yang, et al.
Clinical Genetics|December 4, 2018
Mutations in RELT cause autosomal recessive amelogenesis imperfectaJung-Wook Kim, Hong Zhang, Figen Seymen, et al.
Archives of Oral Biology|June 25, 2013
Genes expressed in dental enamel development are associated with molar-incisor hypomineralizationFabiano Jeremias, Mine Koruyucu, Erika C Küchler, et al.
Oral Diseases|August 28, 2019
Novel frameshift mutations in DSPP cause dentin dysplasia type IIJi Won Lee, Jiwon Hong, Figen Seymen, et al.
European Journal of Oral Sciences|August 19, 2015
Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitionsMerve Bayram, Kathleen Deeley, Maria F Reis, et al.
Molecular Genetics & Genomic Medicine|June 5, 2020
Dental malformations associated with biallelic MMP20 mutationsShih-Kai Wang, Hong Zhang, Michael B Chavez, et al.
Genes|May 28, 2022
The Modified Shields Classification and 12 Families with Defined <i>DSPP</i> MutationsJames P Simmer, Hong Zhang, Sophie J H Moon, et al.
Pageof 9