Sabir, A. H., Ryan, G., Mohammed, Z., Kirk, J., Kiely, N., Thyagarajan, M., & Cole, T. Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case. Wiley.
Chicago Style (17th ed.) CitationSabir, A. H., G. Ryan, Z. Mohammed, J. Kirk, N. Kiely, M. Thyagarajan, and T. Cole. Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case. Wiley.
MLA (9th ed.) CitationSabir, A. H., et al. Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case. Wiley.
Warning: These citations may not always be 100% accurate.