APA (7th ed.) Citation

Jarmolowicz, A. I., Baker, E. K., Bartlett, E., Francis, D., Ling, L., Gamage, D., . . . Godler, D. E. (2021). Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program. American Journal of Medical Genetics. Part A, 185(5), 1498. https://doi.org/10.1002/ajmg.a.62106

Chicago Style (17th ed.) Citation

Jarmolowicz, Anna I., Emma K. Baker, Essra Bartlett, David Francis, Ling Ling, Dinusha Gamage, Martin B. Delatycki, and David E. Godler. "Fragile X Syndrome Full Mutation in Cognitively Normal Male Identified as Part of an Australian Reproductive Carrier Screening Program." American Journal of Medical Genetics. Part A 185, no. 5 (2021): 1498. https://doi.org/10.1002/ajmg.a.62106.

MLA (9th ed.) Citation

Jarmolowicz, Anna I., et al. "Fragile X Syndrome Full Mutation in Cognitively Normal Male Identified as Part of an Australian Reproductive Carrier Screening Program." American Journal of Medical Genetics. Part A, vol. 185, no. 5, 2021, p. 1498, https://doi.org/10.1002/ajmg.a.62106.