UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus

Hoefsloot, LH; Roux, AF; Bitner-Glindzicz, M; (2013) EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus. European Journal of Human Genetics , 21 pp. 1325-1329. 10.1038/ejhg.2013.83. Green open access

[thumbnail of ejhg201383a.pdf]
Preview
PDF
ejhg201383a.pdf

Download (412kB)
Type: Article
Title: EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus
Open access status: An open access version is available from UCL Discovery
DOI: 10.1038/ejhg.2013.83
Publisher version: http://dx.doi.org/10.1038/ejhg.2013.83
Language: English
Additional information: This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/.
UCL classification: UCL
URI: https://discovery.ucl.ac.uk/id/eprint/1418621
Downloads since deposit
275Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item