2012
DOI: 10.4103/0255-0857.96725
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Diagnosis of congenital toxoplasmosis by polymerase chain reaction

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Cited by 6 publications
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“…DNA of 0.5 g of placenta samples were extracted using DNA extraction kit, according to the manufacturer’s instructions (Bioneer, Korea). PCR was carried out to amplify the 400 bp segments of T. gondii by primer G529 with annealing temperature of 48ºC for 30 sec ( 6 ). Forward 5’-TTT TGA CTC GGG CCC AGC 3’; Reverse ; 5'-GTC CAA GCC TCC GAC TCT 3 '.…”
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confidence: 99%
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“…DNA of 0.5 g of placenta samples were extracted using DNA extraction kit, according to the manufacturer’s instructions (Bioneer, Korea). PCR was carried out to amplify the 400 bp segments of T. gondii by primer G529 with annealing temperature of 48ºC for 30 sec ( 6 ). Forward 5’-TTT TGA CTC GGG CCC AGC 3’; Reverse ; 5'-GTC CAA GCC TCC GAC TCT 3 '.…”
mentioning
confidence: 99%
“…The highest prevalence of T. gondii infection was among the age group of 20-29 years and undergraduate and housekeepers women. Based on false negativity in serological data, PCR using the placental tissue is useful for the rapid and accurate diagnosis of congenital toxoplasmosis ( 4 , 6 ). In our study, the rate of T. gondii infection using PCR and G529 primer was 3.67 times higher in the aborted placenta compared to those with normal delivery, but the difference was not significant (P = 0.17).…”
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confidence: 99%