APA citiranje

Hartin, S. N., Hossain, W. A., Francis, D., Godler, D. E., Barkataki, S., & Butler, M. G. (2019). Analysis of the Prader–Willi syndrome imprinting center using droplet digital PCR and next‐generation whole‐exome sequencing. Mol Genet Genomic Med.

Citação norma Chicago

Hartin, Samantha N., Waheeda A. Hossain, David Francis, David E. Godler, Sangjucta Barkataki, and Merlin G. Butler. "Analysis of the Prader–Willi Syndrome Imprinting Center Using Droplet Digital PCR and Next‐generation Whole‐exome Sequencing." Mol Genet Genomic Med 2019.

MLA citiranje

Hartin, Samantha N., et al. "Analysis of the Prader–Willi Syndrome Imprinting Center Using Droplet Digital PCR and Next‐generation Whole‐exome Sequencing." Mol Genet Genomic Med 2019.