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Twenty-year follow-up of a familial case of PTH1R-associated primary failure of tooth eruption

Kanno, Cláudia Misue, Américo de Oliveira, José, Garcia, José Fernando, Roth, Helmut and Weber, Bernhard H. F. (2017) Twenty-year follow-up of a familial case of PTH1R-associated primary failure of tooth eruption. American Journal of Orthodontics and Dentofacial Orthopedics 151 (3), pp. 598-606.

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Abstract

Introduction: Nonsyndromic primary failure of eruption (PFE) is a rare autosomal dominant disorder of dental eruption with no obvious dental or soft tissue interference. The purposes of this study were to genetically and clinically characterize a family with many members affected by PFE and to describe the natural evolution of the disorder. Methods: Three generations of a family with 18 members, ...

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Item type:Article
Date:28 February 2017
Additional Information (public):BIS 19. APRIL 2017 freier Zugriff auf den Volltext über einen "Share Link" möglich: https://authors.elsevier.com/a/1UdvG3AGXGSiSG
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1016/j.ajodo.2016.09.012DOI
28257744PubMed ID
Related URLs:
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Keywords:SECONDARY RETENTION; PERMANENT MOLARS; MUTATIONS; ANKYLOSIS; GENETICS; HUMANS;
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:35435
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