Mcgraw, S., Oakes, C. C., Martel, J., Cirio, M. C., de Zeeuw, P., Mak, W., . . . Trasler, J. M. (2013). Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females. Web
Citación estilo ChicagoMcgraw, Serge, et al. Loss of DNMT1o Disrupts Imprinted X Chromosome Inactivation and Accentuates Placental Defects in Females. 2013.
Cita MLAMcgraw, Serge, et al. Loss of DNMT1o Disrupts Imprinted X Chromosome Inactivation and Accentuates Placental Defects in Females. 2013.
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