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

MLA

Hoefsloot, Lies H., et al. “EMQN Best Practice Guidelines for Diagnostic Testing of Mutations Causing Non-Syndromic Hearing Impairment at the DFNB1 Locus.” European Journal of Human Genetics : EJHG, vol. 21, no. 11, Nov. 2013, pp. 1325–29. EBSCOhost, https://doi.org/10.1038/ejhg.2013.83.

APA

Hoefsloot, L. H., Roux, A.-F., & 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 : EJHG, 21(11), 1325–1329. https://doi.org/10.1038/ejhg.2013.83

Chicago

Hoefsloot, Lies H, Anne-Françoise Roux, and Maria Bitner-Glindzicz. 2013. “EMQN Best Practice Guidelines for Diagnostic Testing of Mutations Causing Non-Syndromic Hearing Impairment at the DFNB1 Locus.” European Journal of Human Genetics : EJHG 21 (11): 1325–29. doi:10.1038/ejhg.2013.83.