Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal‐onset Cockayne syndrome features.

MLA

Ricotti, R., et al. “Phenotypic Variability in Xeroderma Pigmentosum Group G: An Uncommon Case with Severe Prenatal‐onset Cockayne Syndrome Features.” Clinical Genetics, vol. 94, no. 3/4, Oct. 2018, pp. 386–88. EBSCOhost, https://doi.org/10.1111/cge.13364.

APA

Ricotti, R., Nardo, T., Striano, P., Stefanini, M., Orioli, D., & Botta, E. (2018). Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal‐onset Cockayne syndrome features. Clinical Genetics, 94(3/4), 386–388. https://doi.org/10.1111/cge.13364

Chicago

Ricotti, R., T. Nardo, P. Striano, M. Stefanini, D. Orioli, and E. Botta. 2018. “Phenotypic Variability in Xeroderma Pigmentosum Group G: An Uncommon Case with Severe Prenatal‐onset Cockayne Syndrome Features.” Clinical Genetics 94 (3/4): 386–88. doi:10.1111/cge.13364.