Placental chimerism in early human pregnancy.

dc.contributor.authorHalder, Ashutosh
dc.date.accessioned2012-11-26T09:34:38Z
dc.date.available2012-11-26T09:34:38Z
dc.date.issued2005-05
dc.description.abstractBackground0 : Human chimerism is rare and usually uncovered through investigations of ambiguous genitalia or blood grouping or prenatal diagnosis. Most of the publications on placental chimerism are mainly case reports. There is no systematic search with sensitive techniques for placental chimerism in human. Aim0 : This study was aimed to asses placental chimerism through two sensitive molecular techniques i.e., interphase fluorescent in situ hybridization and quantitative fluorescent PCR. Material and methods0 : Placental chimerism was analyzed using X & Y dual color fluorescent in-situ hybridization onto 154 placentae from natural conceptions, obtained at termination of pregnancy between 7 to 16 weeks of gestation. Results0 : Three cases of placental sex chromosome chimerism were observed (1.95%). Exclusion of maternal contamination and diagnosis was confirmed later by quantitative fluorescent PCR. Conclusion0 : This finding indicates that placental chimerism in early human pregnancy is not rare.en_US
dc.identifier.citationHalder Ashutosh. Placental chimerism in early human pregnancy. Indian Journal of Human Genetics. 2005 May; 11(2): 84-88.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/143335
dc.language.isoenen_US
dc.source.urihttps://www.ijhg.com/article.asp?issn=0971-6866;year=2005;volume=11;issue=2;spage=84;epage=88;aulast=Ashutoshen_US
dc.subjectPlacental Chimerismen_US
dc.subjectInterphase FISH & Quantitative Fluorescent PCRen_US
dc.titlePlacental chimerism in early human pregnancy.en_US
dc.typeArticleen_US
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