<i>WNT10A</i> and <i>RUNX2</i> mutations associated with non‐syndromic tooth agenesis-Reference-Cited by-同舟云学术

WNT10A and RUNX2 mutations associated with non‐syndromic tooth agenesis

Published:2022-10-17 Issue:6 Volume:130 Page:
ISSN:0909-8836
Container-title:European Journal of Oral Sciences
language:en
Short-container-title:European J Oral Sciences

Author:

Živković Marija¹^ORCID,Stefanović Neda¹^ORCID,Glišić Branislav¹^ORCID,Brajović Gavrilo²^ORCID,Miličić Biljana³^ORCID,Kostić Marija⁴^ORCID,Popović Branka⁵^ORCID

Affiliation:

1. Department of Orthodontics University of Belgrade School of Dental Medicine Belgrade Serbia

2. Department of Physiology University of Belgrade School of Dental Medicine Belgrade Serbia

3. Department for Medical Statistics and Informatics University of Belgrade School of Dental Medicine Belgrade Serbia

4. Faculty of Hotel Management and Tourism University of Kragujevac Vrnjacka Banja Serbia

5. Department of Human Genetics University of Belgrade School of Dental Medicine Belgrade Serbia

Funder

Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja

Publisher

Wiley

Subject

General Dentistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/eos.12896

Reference45 articles.

1. Congenitally missing teeth (hypodontia): A review of the literature concerning the etiology, prevalence, risk factors, patterns and treatment

2. Prevalence of hypodontia and associated factors: a systematic review and meta-analysis

3. Multilevel complex interactions between genetic, epigenetic and environmental factors in the aetiology of anomalies of dental development

4. The genetic basis of tooth development and dental defects

5. Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis

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1. Exploring the association between PITX2, third molars agenesis and sella turcica morphology;Head & Face Medicine;2024-02-28

2. Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family;Archives of Oral Biology;2023-10