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:	Science & Technology Life Sciences & Biomedicine Biochemistry & Molecular Biology Medicine, Research & Experimental Research & Experimental Medicine MULTIPLE DISPLACEMENT AMPLIFICATION FULL-MUTATION PRIMED PCR PRACTICE GUIDELINES MYOTONIC-DYSTROPHY EXPANDED ALLELES PREMUTATION DNA CARRIERS DISEASE
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/226868
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Institution:	National University of Singapore
Language:	English

id	sg-nus-scholar.10635-226868
record_format	dspace
spelling	sg-nus-scholar.10635-2268682024-04-24T03:01:23Z 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 SH Chen, Min Tan, Arnold SC Prasath, Ethiraj B Loh, Seong Feei Chong, Samuel S PAEDIATRICS DUKE-NUS MEDICAL SCHOOL Science & Technology Life Sciences & Biomedicine Biochemistry & Molecular Biology Medicine, Research & Experimental Research & Experimental Medicine MULTIPLE DISPLACEMENT AMPLIFICATION FULL-MUTATION PRIMED PCR PRACTICE GUIDELINES MYOTONIC-DYSTROPHY EXPANDED ALLELES PREMUTATION DNA CARRIERS DISEASE 10.1017/erm.2017.10 EXPERT REVIEWS IN MOLECULAR MEDICINE 19 2022-06-09T06:48:48Z 2022-06-09T06:48:48Z 2017-07-19 2022-06-07T06:54:35Z Review Rajan-Babu, Indhu-Shree, Lian, Mulias, Cheah, Felicia SH, Chen, Min, Tan, Arnold SC, Prasath, Ethiraj B, Loh, Seong Feei, Chong, Samuel S (2017-07-19). FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome. EXPERT REVIEWS IN MOLECULAR MEDICINE 19. ScholarBank@NUS Repository. https://doi.org/10.1017/erm.2017.10 14623994 https://scholarbank.nus.edu.sg/handle/10635/226868 en CAMBRIDGE UNIV PRESS Elements
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
language	English
topic	Science & Technology Life Sciences & Biomedicine Biochemistry & Molecular Biology Medicine, Research & Experimental Research & Experimental Medicine MULTIPLE DISPLACEMENT AMPLIFICATION FULL-MUTATION PRIMED PCR PRACTICE GUIDELINES MYOTONIC-DYSTROPHY EXPANDED ALLELES PREMUTATION DNA CARRIERS DISEASE
spellingShingle	Science & Technology Life Sciences & Biomedicine Biochemistry & Molecular Biology Medicine, Research & Experimental Research & Experimental Medicine MULTIPLE DISPLACEMENT AMPLIFICATION FULL-MUTATION PRIMED PCR PRACTICE GUIDELINES MYOTONIC-DYSTROPHY EXPANDED ALLELES PREMUTATION DNA CARRIERS DISEASE Rajan-Babu, Indhu-Shree Lian, Mulias Cheah, Felicia SH Chen, Min Tan, Arnold SC Prasath, Ethiraj B Loh, Seong Feei Chong, Samuel S FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
description	10.1017/erm.2017.10
author2	PAEDIATRICS
author_facet	PAEDIATRICS Rajan-Babu, Indhu-Shree Lian, Mulias Cheah, Felicia SH Chen, Min Tan, Arnold SC Prasath, Ethiraj B Loh, Seong Feei Chong, Samuel S
format	Review
author	Rajan-Babu, Indhu-Shree Lian, Mulias Cheah, Felicia SH Chen, Min Tan, Arnold SC Prasath, Ethiraj B Loh, Seong Feei Chong, Samuel S
author_sort	Rajan-Babu, Indhu-Shree
title	FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
title_short	FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
title_full	FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
title_fullStr	FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
title_full_unstemmed	FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
title_sort	fmr1 cgg repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile x syndrome
publisher	CAMBRIDGE UNIV PRESS
publishDate	2022
url	https://scholarbank.nus.edu.sg/handle/10635/226868
_version_	1800915422940233728

FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

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