APA引文

Rajan-Babu, I., Lian, M., Cheah, F. S., Chen, M., Tan, A. S., Prasath, E. B., . . . SCHOOL, D. M. (2022). FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome. CAMBRIDGE UNIV PRESS.

Chicago Style Citation

Rajan-Babu, Indhu-Shree, Mulias Lian, Felicia SH Cheah, Min Chen, Arnold SC Tan, Ethiraj B. Prasath, Seong Feei Loh, Samuel S. Chong, and DUKE-NUS MEDICAL SCHOOL. FMR1 CGG Repeat Expansion Mutation Detection and Linked Haplotype Analysis for Reliable and Accurate Preimplantation Genetic Diagnosis of Fragile X Syndrome. CAMBRIDGE UNIV PRESS, 2022.

MLA引文

Rajan-Babu, Indhu-Shree, et al. FMR1 CGG Repeat Expansion Mutation Detection and Linked Haplotype Analysis for Reliable and Accurate Preimplantation Genetic Diagnosis of Fragile X Syndrome. CAMBRIDGE UNIV PRESS, 2022.