A single common assay for robust and rapid fragile X mental retardation syndrome screening from dried blood spots
10.3389/fgene.2018.00582
Saved in:
Main Authors: | Tan, V.J., Lian, M., Faradz, S.M.H., Winarni, T.I.., Chong, S.S. |
---|---|
Other Authors: | PAEDIATRICS |
Format: | Article |
Published: |
Frontiers Media S.A.
2021
|
Subjects: | |
Online Access: | https://scholarbank.nus.edu.sg/handle/10635/210906 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
DEVELOPMENT OF INNOVATIVE MOLECULAR AND SINGLE-CELL PREIMPLANTATION GENETIC DIAGNOSTIC AND SCREENING TESTS FOR DETECTING CGG-REPEAT EXPANSIONS IN THE FMR1 GENE
by: RAJAN BABU INDHU SHREE
Published: (2016) -
Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
by: ZHOU YOUYOU
Published: (2010) -
Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 gene
by: Lim G.X.Y., et al.
Published: (2020) -
Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias
by: Lian, Mulias, et al.
Published: (2022) -
Neurodegenerative diseases associated with non-coding CGG tandem repeat expansions
by: Zhou, Zhidong, et al.
Published: (2022)