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

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Bibliographic Details
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:
DNA
Online Access:https://scholarbank.nus.edu.sg/handle/10635/226868
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Institution: National University of Singapore
Language: English
Description
Summary:10.1017/erm.2017.10