APA (7th ed.) Citation

Wieland, I., Weidner, C., Ciccone, R., Lapi, E., McDonald-McGinn, D., Kress, W., . . . Wieacker, P. (2007). Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome. Clinical Genetics, 72(6), 506. https://doi.org/10.1111/j.1399-0004.2007.00905.x

Chicago Style (17th ed.) Citation

Wieland, I., et al. "Contiguous Gene Deletions Involving EFNB1, OPHN1, PJA1 and EDA in Patients with Craniofrontonasal Syndrome." Clinical Genetics 72, no. 6 (2007): 506. https://doi.org/10.1111/j.1399-0004.2007.00905.x.

MLA (9th ed.) Citation

Wieland, I., et al. "Contiguous Gene Deletions Involving EFNB1, OPHN1, PJA1 and EDA in Patients with Craniofrontonasal Syndrome." Clinical Genetics, vol. 72, no. 6, 2007, p. 506, https://doi.org/10.1111/j.1399-0004.2007.00905.x.