APA (7th ed.) Citation

Bonsch, D., Neumann, C., Lang-Roth, R., Witte, O., Lamprecht-Dinnesen, A., & Deufel, T. (2003). PROMM and deafness: Exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype. Clinical Genetics, 63(1), 73. https://doi.org/10.1034/j.1399-0004.2003.630112.x

Chicago Style (17th ed.) Citation

Bonsch, D., C. Neumann, R. Lang-Roth, O. Witte, A. Lamprecht-Dinnesen, and T. Deufel. "PROMM and Deafness: Exclusion of ZNF9 as the Disease Gene in DFNA18 Suggests a Polygenic Origin of the PROMM/DM2 Phenotype." Clinical Genetics 63, no. 1 (2003): 73. https://doi.org/10.1034/j.1399-0004.2003.630112.x.

MLA (9th ed.) Citation

Bonsch, D., et al. "PROMM and Deafness: Exclusion of ZNF9 as the Disease Gene in DFNA18 Suggests a Polygenic Origin of the PROMM/DM2 Phenotype." Clinical Genetics, vol. 63, no. 1, 2003, p. 73, https://doi.org/10.1034/j.1399-0004.2003.630112.x.