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PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption

Decker, W., Stellzig-Eisenhauer, A., Fiebig, B. S., Rau, C., Kress, W., Saar, K., Rüschendorf, F., Hubner, N., Grimm, T. and Weber, Bernhard H. F. (2008) PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption. American Journal of Human Genetics 83, pp. 781-786.

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Abstract

Tooth eruption is a complex developmental process requiring coordinated navigation through alveolar bone and oral epithelium. Primary failure of tooth eruption (PFE) is associated with several syndromes primarily affecting skeletal development, but it is also known as a nonsyndromic autosomal-dominant condition. Teeth in the posterior quadrants of the upper and lower jaw are preferentially ...

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Item type:Article
Date:2008
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1016/j.ajhg.2008.11.006DOI
19061984PubMed ID
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:35204
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