Characteristic dental pattern with hypodontia and short roots in Fraser syndrome-Reference-Cited by-同舟云学术

Characteristic dental pattern with hypodontia and short roots in Fraser syndrome

Published:2020-06-02 Issue:7 Volume:182 Page:1681-1689
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Kunz Felix¹,Kayserili Hülya²^ORCID,Midro Alina³^ORCID,Silva Deepthi⁴,Basnayake Sriyani⁵,Güven Yeliz⁶,Borys Jan⁷,Schanze Denny⁸,Stellzig‐Eisenhauer Angelika¹,Bloch‐Zupan Agnes⁹¹⁰¹¹^ORCID,Zenker Martin⁸^ORCID

Affiliation:

1. Department of Orthodontics University Hospital of Würzburg Würzburg Germany

2. KOÇ University School of Medicine (KUSoM) Medical Genetics Department Topkapi Zeytinburnu Istanbul Turkey

3. Department of Clinical Genetics Medical University Białystok Poland

4. Department of Physiology, Faculty of Medicine University of Kelaniya Ragama Sri Lanka

5. Orthodontic Unit Lady Ridgway Hospital Colombo Sri Lanka

6. Department of Pedodontics, Faculty of Dentistry Istanbul University Istanbul Turkey

7. Department of Maxillofacial and Plastic Surgery Medical University of Bialystok Poland

8. Institute of Human Genetics, University Hospital Magdeburg Germany

9. Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM U1258, CNRS‐UMR7104, Université de Strasbourg Illkirch‐Graffenstaden France

10. Hôpitaux Universitaires de Strasbourg (HUS), Pôle de Médecine et Chirurgie Bucco‐Dentaires, Hôpital Civil, Centre de référence des maladies rares orales et dentaires, O‐Rares, Filière Santé Maladies rares TETE COU, European Reference Network ERN CRANIO Strasbourg France

11. Faculté de Chirurgie Dentaire Université de Strasbourg Strasbourg France

Funder

European Regional Development Fund

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61610

Reference24 articles.

1. FREM1 Mutations Cause Bifid Nose, Renal Agenesis, and Anorectal Malformations Syndrome

2. Nephronectin plays critical roles in Sox2 expression and proliferation in dental epithelial stem cells via EGF-like repeat domains