APA (7th ed.) Citation

Neuhaus, C., Lang‐Roth, R., Zimmermann, U., Heller, R., Eisenberger, T., Weikert, M., . . . Bolz, H. (2017). Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1). Clinical Genetics, 91(6), 892. https://doi.org/10.1111/cge.12915

Chicago Style (17th ed.) Citation

Neuhaus, C., R. Lang‐Roth, U. Zimmermann, R. Heller, T. Eisenberger, M. Weikert, S. Markus, M. Knipper, and H.J Bolz. "Extension of the Clinical and Molecular Phenotype of DIAPH1-associated Autosomal Dominant Hearing Loss ( DFNA1)." Clinical Genetics 91, no. 6 (2017): 892. https://doi.org/10.1111/cge.12915.

MLA (9th ed.) Citation

Neuhaus, C., et al. "Extension of the Clinical and Molecular Phenotype of DIAPH1-associated Autosomal Dominant Hearing Loss ( DFNA1)." Clinical Genetics, vol. 91, no. 6, 2017, p. 892, https://doi.org/10.1111/cge.12915.