Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation G...

por Zhao, Mingjue, Lian, Mulias, Cheah, Felicia S.H., Tan, Arnold S.C., Agarwal, Anupriya, Chong, Samuel S.
Publicado 2019

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

Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric i...

por Nguyen, Minh Tam, Nguyen, Thanh Tung, Nguyen, Duy Bac, Nguyen, Thi Mai, Nguyen, Kim Ngan, Ngo, Van Nhat Minh, Nguyen, Van Dieu, Tran, Ngoc Anh, Lian, Mulias, Tan, Arnold S. C., Chong, Samuel S., Dang, Tien Truong
Publicado 2023