The discovery of human genetic variations and their use as disease markers: Past, present and future

10.1038/jhg.2010.55

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Bibliographic Details
Main Authors:	Ku, C.S., Loy, E.Y., Salim, A., Pawitan, Y., Chia, K.S.
Other Authors:	CENTRE FOR MOLECULAR EPIDEMIOLOGY
Format:	Review
Published:	2014
Subjects:	copy number variations genome-wide association studies human genetic variations indels loss of heterozygosity restriction fragment length polymorphisms single nucleotide polymorphisms tandem repeats
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/108693
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1086932023-10-26T09:46:36Z The discovery of human genetic variations and their use as disease markers: Past, present and future Ku, C.S. Loy, E.Y. Salim, A. Pawitan, Y. Chia, K.S. CENTRE FOR MOLECULAR EPIDEMIOLOGY EPIDEMIOLOGY & PUBLIC HEALTH copy number variations genome-wide association studies human genetic variations indels loss of heterozygosity restriction fragment length polymorphisms single nucleotide polymorphisms tandem repeats 10.1038/jhg.2010.55 Journal of Human Genetics 55 7 403-415 JHGEF 2014-11-25T09:49:07Z 2014-11-25T09:49:07Z 2010-07 Review Ku, C.S., Loy, E.Y., Salim, A., Pawitan, Y., Chia, K.S. (2010-07). The discovery of human genetic variations and their use as disease markers: Past, present and future. Journal of Human Genetics 55 (7) : 403-415. ScholarBank@NUS Repository. https://doi.org/10.1038/jhg.2010.55 14345161 http://scholarbank.nus.edu.sg/handle/10635/108693 000280326700003 Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	copy number variations genome-wide association studies human genetic variations indels loss of heterozygosity restriction fragment length polymorphisms single nucleotide polymorphisms tandem repeats
spellingShingle	copy number variations genome-wide association studies human genetic variations indels loss of heterozygosity restriction fragment length polymorphisms single nucleotide polymorphisms tandem repeats Ku, C.S. Loy, E.Y. Salim, A. Pawitan, Y. Chia, K.S. The discovery of human genetic variations and their use as disease markers: Past, present and future
description	10.1038/jhg.2010.55
author2	CENTRE FOR MOLECULAR EPIDEMIOLOGY
author_facet	CENTRE FOR MOLECULAR EPIDEMIOLOGY Ku, C.S. Loy, E.Y. Salim, A. Pawitan, Y. Chia, K.S.
format	Review
author	Ku, C.S. Loy, E.Y. Salim, A. Pawitan, Y. Chia, K.S.
author_sort	Ku, C.S.
title	The discovery of human genetic variations and their use as disease markers: Past, present and future
title_short	The discovery of human genetic variations and their use as disease markers: Past, present and future
title_full	The discovery of human genetic variations and their use as disease markers: Past, present and future
title_fullStr	The discovery of human genetic variations and their use as disease markers: Past, present and future
title_full_unstemmed	The discovery of human genetic variations and their use as disease markers: Past, present and future
title_sort	discovery of human genetic variations and their use as disease markers: past, present and future
publishDate	2014
url	http://scholarbank.nus.edu.sg/handle/10635/108693
_version_	1781788558934147072

The discovery of human genetic variations and their use as disease markers: Past, present and future

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