Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2

Master's

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Bibliographic Details
Main Author:	ZHOU YOUYOU
Other Authors:	PAEDIATRICS
Format:	Theses and Dissertations
Language:	English
Published:	2010
Subjects:	trinucleotide repeat disease; fragile X syndrome; CGG repeat; methylation-specific PCR;
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/13474
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Institution:	National University of Singapore
Language:	English

id	sg-nus-scholar.10635-13474
record_format	dspace
spelling	sg-nus-scholar.10635-134742015-01-05T17:58:12Z Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2 ZHOU YOUYOU PAEDIATRICS CHONG SIONG-CHUAN, SAMUEL trinucleotide repeat disease; fragile X syndrome; CGG repeat; methylation-specific PCR; Master's MASTER OF SCIENCE 2010-04-08T10:33:20Z 2010-04-08T10:33:20Z 2004-01-13 Thesis ZHOU YOUYOU (2004-01-13). Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2. ScholarBank@NUS Repository. http://scholarbank.nus.edu.sg/handle/10635/13474 NOT_IN_WOS en
institution	National University of Singapore
building	NUS Library
country	Singapore
collection	ScholarBank@NUS
language	English
topic	trinucleotide repeat disease; fragile X syndrome; CGG repeat; methylation-specific PCR;
spellingShingle	trinucleotide repeat disease; fragile X syndrome; CGG repeat; methylation-specific PCR; ZHOU YOUYOU Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
description	Master's
author2	PAEDIATRICS
author_facet	PAEDIATRICS ZHOU YOUYOU
format	Theses and Dissertations
author	ZHOU YOUYOU
author_sort	ZHOU YOUYOU
title	Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
title_short	Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
title_full	Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
title_fullStr	Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
title_full_unstemmed	Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2
title_sort	molecular genetic studies of fragile x syndrome and spinocerebellar ataxia type 2
publishDate	2010
url	http://scholarbank.nus.edu.sg/handle/10635/13474
_version_	1681078863931637760

Molecular genetic studies of fragile X syndrome and spinocerebellar ataxia type 2

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