APA aipamena

Luo, S., Huang, W., Xia, Q., Xia, Y., Du, Q., Wu, L., & Duan, R. (2014). Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: Case report. BMC Med Genet.

Chicago Style aipamena

Luo, Shiyu, Wen Huang, Qiuping Xia, Yan Xia, Qian Du, Lingqian Wu, and Ranhui Duan. "Cryptic FMR1 Mosaic Deletion in a Phenotypically Normal Mother of a Boy With Fragile X Syndrome: Case Report." BMC Med Genet 2014.

MLA aipamena

Luo, Shiyu, et al. "Cryptic FMR1 Mosaic Deletion in a Phenotypically Normal Mother of a Boy With Fragile X Syndrome: Case Report." BMC Med Genet 2014.