Cita APA (7a ed.)

Lu, G., Peng, Q., Wu, L., Zhang, J., & Ma, L. (2021). Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin–Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing. BMC.

Cita Chicago Style (17a ed.)

Lu, Guanting, Qiongling Peng, Lianying Wu, Jian Zhang, y Liya Ma. Identification of De Novo Mutations for ARID1B Haploinsufficiency Associated with Coffin–Siris Syndrome 1 in Three Chinese Families via Array-CGH and Whole Exome Sequencing. BMC, 2021.

Cita MLA (8a ed.)

Lu, Guanting, et al. Identification of De Novo Mutations for ARID1B Haploinsufficiency Associated with Coffin–Siris Syndrome 1 in Three Chinese Families via Array-CGH and Whole Exome Sequencing. BMC, 2021.