APA (7th ed.) Citation

Hoefsloot, L. H., Roux, A., & 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(11), 1325. https://doi.org/10.1038/ejhg.2013.83

Chicago Style (17th ed.) Citation

Hoefsloot, Lies H., Anne-Françoise Roux, and Maria Bitner-Glindzicz. "EMQN Best Practice Guidelines for Diagnostic Testing of Mutations Causing Non-syndromic Hearing Impairment at the DFNB1 Locus." European Journal of Human Genetics 21, no. 11 (2013): 1325. https://doi.org/10.1038/ejhg.2013.83.

MLA (9th ed.) Citation

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, vol. 21, no. 11, 2013, p. 1325, https://doi.org/10.1038/ejhg.2013.83.