In April 2016 Manchester eScholar was replaced by the University of Manchester’s
new Research Information Management System, Pure. In the autumn the University’s research
outputs will be available to search and browse via a new Research Portal. Until then
the University’s full publication record can be accessed via a
temporary portal and the old eScholar content is available to search and browse via this archive.
Related resources
Full-text held externally
Search for item elsewhere
University researcher(s)
Academic department(s)
Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome
O'Sullivan, J; Bitu, C C; Daly, S B; Urquhart, J E; Barron, M J; Bhaskar, S S; Martelli-Junior, H; dos Santos Neto, P E; Mansilla, M A; Murray, J C; Coletta, R D; Black, G CM; Dixon, M J
American Journal of Human Genetics . 2011;88(5):616-620.
Access to files
Full-text and supplementary files are not available from Manchester eScholar. Full-text is available externally using the following links:
Full-text held externally
Bibliographic metadata
Type of resource:
Content type:
Publication form:
Author(s):
Published date:
Article title:
Journal title:
ISSN:
Publisher:
Volume:
88
Issue:
5
Start page:
616
End page:
620
Total:
5
Digital Object Identifier:
10.1016/j.ajhg.2011.04.005
ISI Accession Number:
000290832100009
Access state:
Active
Institutional metadata
University researcher(s):
Academic department(s):
Record metadata
Manchester eScholar ID:
uk-ac-man-scw:126093
Created by:
Black, Graeme
Created:
5th July, 2011, 16:19:56
Last modified by:
Bentley, Hazel
Last modified:
21st January, 2015, 08:18:17