Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/107571
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dc.titleGonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis
dc.contributor.authorGole, L.A.
dc.contributor.authorLim, J.
dc.contributor.authorCrolla, J.A.
dc.contributor.authorLoke, K.Y.
dc.date.accessioned2014-11-06T08:59:41Z
dc.date.available2014-11-06T08:59:41Z
dc.date.issued2008-04
dc.identifier.citationGole, L.A.,Lim, J.,Crolla, J.A.,Loke, K.Y. (2008-04). Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis. Singapore Medical Journal 49 (4) : 349-351. ScholarBank@NUS Repository.
dc.identifier.issn00375675
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/107571
dc.description.abstractA two-year-and-eight-month-old girl presented with clitoromegaly and short stature. Two cell lines, 45,X and 46,X,idic(Y)(q11.2), were observed. Cytogenetic and fluorescence in situ hybridisation investigations were carried out on her peripheral lymphocytes and gonadal cells, to determine the genotype-phenotype effect with respect to differential tissue distribution, effects of the sex determining region of the Y chromosome, and the break-points in the azoospermia factor region.
dc.sourceScopus
dc.subjectFluorescence in situ hybridisation
dc.subjectGonadal dysgenesis
dc.subjectMosaicism
dc.subjectSex chromosome aberrations
dc.subjectTurner syndrome
dc.typeArticle
dc.contributor.departmentOBSTETRICS & GYNAECOLOGY
dc.contributor.departmentPAEDIATRICS
dc.description.sourcetitleSingapore Medical Journal
dc.description.volume49
dc.description.issue4
dc.description.page349-351
dc.description.codenSIMJA
dc.identifier.isiutNOT_IN_WOS
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