FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
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.Volume:
19
Year:
2017
Language:
english
Journal:
Expert Reviews in Molecular Medicine
DOI:
10.1017/erm.2017.10
File:
PDF, 1.90 MB
english, 2017