FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

by Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia SH, Chen, Min, Tan, Arnold SC, Prasath, Ethiraj B, Loh, Seong Feei, Chong, Samuel S
Published 2022

Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR

by Liu, Timing, Wang, Furene S, Cheah, Felicia SH, Gu, Yanghong, Shaw, Marie, Law, Hai-Yang, Tay, Stacey KH, Lee, Caroline G, Nelson, David L, Gecz, Jozef, Chong, Samuel S
Published 2021