Demond, H., Anvar, Z., Jahromi, B. N., Sparago, A., Verma, A., Davari, M., . . . Kelsey, G. (2019). A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation.
Chicago Style CitationDemond, Hannah, et al. A KHDC3L Mutation Resulting in Recurrent Hydatidiform Mole Causes Genome-wide DNA Methylation Loss in Oocytes and Persistent Imprinting Defects Post-fertilisation. 2019.
MLA CitationDemond, Hannah, et al. A KHDC3L Mutation Resulting in Recurrent Hydatidiform Mole Causes Genome-wide DNA Methylation Loss in Oocytes and Persistent Imprinting Defects Post-fertilisation. 2019.
Warning: These citations may not always be 100% accurate.