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Please use this identifier to cite or link to this item: https://doi.org/10.1373/clinchem.2006.068593
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dc.titleSimplified molecular diagnosis of fragile X syndrome by fluorescent methylation-specific PCR and GeneScan analysis
dc.contributor.authorZhou, Y.
dc.contributor.authorLum, J.M.S.
dc.contributor.authorYeo, G.-H.
dc.contributor.authorTay, S.K.H.
dc.contributor.authorChong, S.S.
dc.contributor.authorKiing, J.
dc.date.accessioned2011-08-16T07:42:13Z
dc.date.available2011-08-16T07:42:13Z
dc.date.issued2006
dc.identifier.citationZhou, Y., Lum, J.M.S., Yeo, G.-H., Tay, S.K.H., Chong, S.S., Kiing, J. (2006). Simplified molecular diagnosis of fragile X syndrome by fluorescent methylation-specific PCR and GeneScan analysis. Clinical Chemistry 52 (8) : 1492-1500. ScholarBank@NUS Repository. https://doi.org/10.1373/clinchem.2006.068593
dc.identifier.issn00099147
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/25633
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1373/clinchem.2006.068593
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1373/clinchem.2006.068593
dc.description.sourcetitleClinical Chemistry
dc.description.volume52
dc.description.issue8
dc.description.page1492-1500
dc.identifier.isiut000239480300006
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