uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus.
2013 (English)In: European Journal of Human Genetics, ISSN 1018-4813, E-ISSN 1476-5438, Vol. 21, no 11, 1325-1329 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2013. Vol. 21, no 11, 1325-1329 p.
National Category
Medical Genetics Basic Medicine
Research subject
Clinical Genetics
Identifiers
URN: urn:nbn:se:uu:diva-223937DOI: 10.1038/ejhg.2013.83OAI: oai:DiVA.org:uu-223937DiVA: diva2:714489
Note

Collaborator: Marie-Louise Bondeson, Institutionen för immunologi, genetik och patologi, Medicinsk genetik; Uppsala, Sweden

Available from: 2014-04-28 Created: 2014-04-28 Last updated: 2017-12-05Bibliographically approved

Open Access in DiVA

No full text

Other links

Publisher's full text
In the same journal
European Journal of Human Genetics
Medical GeneticsBasic Medicine

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 358 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf