Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/26068
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dc.titleRefining quantitative fluorescent polymerase chain reaction for prenatal detection of X chromosomal anomalies in the major Southeast Asian populations
dc.contributor.authorGole, L.
dc.contributor.authorNg, B.L.
dc.contributor.authorBaig, S.
dc.contributor.authorBiswas, A.
dc.contributor.authorChoolani, M.
dc.contributor.authorAdrianne, F.
dc.contributor.authorEe, A.M.
dc.contributor.authorKoay, E.
dc.date.accessioned2011-09-15T08:43:02Z
dc.date.available2011-09-15T08:43:02Z
dc.date.issued2008
dc.identifier.citationGole, L.,Ng, B.L.,Baig, S.,Biswas, A.,Choolani, M.,Adrianne, F.,Ee, A.M.,Koay, E. (2008). Refining quantitative fluorescent polymerase chain reaction for prenatal detection of X chromosomal anomalies in the major Southeast Asian populations. Singapore Medical Journal 49 (12) : 1025-1028. ScholarBank@NUS Repository.
dc.identifier.issn00375675
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/26068
dc.sourceScopus
dc.subjectAmniotic fluid samples
dc.subjectCytogenetics
dc.subjectPrenatal diagnosis
dc.subjectQuantitative fluorescent polymerase chain reaction
dc.subjectTurner syndrome
dc.subjectX chromosome abnormalities
dc.typeArticle
dc.contributor.departmentOBSTETRICS & GYNAECOLOGY
dc.contributor.departmentPATHOLOGY
dc.description.sourcetitleSingapore Medical Journal
dc.description.volume49
dc.description.issue12
dc.description.page1025-1028
dc.identifier.isiutNOT_IN_WOS
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