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

por Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia S.H., Chen, Min, Tan, Arnold S.C., Prasath, Ethiraj B., Loh, Seong Feei, Chong, Samuel S.
Publicado 2017