FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
10.1017/erm.2017.10
Saved in:
Main Authors: | Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia SH, Chen, Min, Tan, Arnold SC, Prasath, Ethiraj B, Loh, Seong Feei, Chong, Samuel S |
---|---|
Other Authors: | PAEDIATRICS |
Format: | Review |
Language: | English |
Published: |
CAMBRIDGE UNIV PRESS
2022
|
Subjects: | |
Online Access: | https://scholarbank.nus.edu.sg/handle/10635/226868 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Language: | English |
Similar Items
-
Identification of microsatellite markers < 1 Mb from the FMR1 CGG repeat and development of a single-tube tetradecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of fragile X syndrome
by: Chen, Min, et al.
Published: (2022) -
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) -
Robust preimplantation genetic testing strategy for myotonic dystrophy type 1 by bidirectional triplet-primed polymerase chain reaction combined with multi-microsatellite haplotyping following whole-genome amplification
by: Lian, M., et al.
Published: (2021) -
High-Throughput Methylation-Specific Triplet-Primed PCR and Melting Curve Analysis for Selective and Reliable Identification of Actionable FMR1 Genotypes
by: Rajan-Babu, Indhu-Shree, et al.
Published: (2022) -
Defining the Performance Parameters of a Rapid Screening Tool for FMR1 CGG-Repeat Expansions Based on Direct Triplet-Primed PCR and Melt Curve Analysis
by: Rajan-Babu, Indhu-Shree, et al.
Published: (2022)