Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis

MLA

Moise L. Levy, et al. “Prenatal Diagnosis for Keratin Mutations to Exclude Transmission of Epidermolytic Hyperkeratosis.” Prenatal Diagnosis, vol. 18, Aug. 1998, pp. 826–30. EBSCOhost, https://doi.org/10.1002/(sici)1097-0223(199808)18:8<826::aid-pd360>3.0.co;2-5.

APA

Moise L. Levy, Paul G. Hazen, Michael T. Lin, Dennis R. Roop, Joseph A. Rothnagel, Rhanda A. Holder, & Mary A. Longley. (1998). Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis. Prenatal Diagnosis, 18, 826–830. https://doi.org/10.1002/(sici)1097-0223(199808)18:8<826::aid-pd360>3.0.co;2-5

Chicago

Moise L. Levy, Paul G. Hazen, Michael T. Lin, Dennis R. Roop, Joseph A. Rothnagel, Rhanda A. Holder, and Mary A. Longley. 1998. “Prenatal Diagnosis for Keratin Mutations to Exclude Transmission of Epidermolytic Hyperkeratosis.” Prenatal Diagnosis 18 (August): 826–30. doi:10.1002/(sici)1097-0223(199808)18:8<826::aid-pd360>3.0.co;2-5.