Literature DB >> 10464615

A simple VNTR-PCR method for detecting maternal cell contamination in prenatal diagnosis.

J R Batanian1, D H Ledbetter, R G Fenwick.   

Abstract

The effectiveness of variable number tandem repeats (VNTRs) was evaluated in the detection of maternal cell contamination. Nonradioactive PCRs were performed on 30 sets of prenatal tissue using VNTRs as primers. The combination of two VNTRs (YNZ22 and APOB) provided information on all 30 cases, distinguishing maternal-fetal genotype patterns and detecting maternal cell contamination in 5 of 30 prenatal cases. The amplification of these two VNTRs does not require radioactive or fluorescence labeling, and a small gel electrophoresis is sufficient to see the maternal-fetal genotype pattern. By this method, detection of maternal cell contamination in prenatal tissues can be obtained in 1 day, without the use of expensive instruments, thus providing DNA laboratories a very sensitive, rapid, and simple proof pretest on all prenatal tissues before performing the final genetic diagnostic testing.

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Year:  1998        PMID: 10464615     DOI: 10.1089/gte.1998.2.347

Source DB:  PubMed          Journal:  Genet Test        ISSN: 1090-6576


  4 in total

1.  A one-step real-time PCR assay for rapid prenatal diagnosis of sickle cell disease and detection of maternal contamination.

Authors:  Catherine Costa; Serge Pissard; Emmanuelle Girodon; Danièle Huot; Michel Goossens
Journal:  Mol Diagn       Date:  2003

2.  Testing for maternal cell contamination in prenatal samples: a comprehensive survey of current diagnostic practices in 35 molecular diagnostic laboratories.

Authors:  Iris Schrijver; Sarah C Cherny; James L Zehnder
Journal:  J Mol Diagn       Date:  2007-07       Impact factor: 5.568

3.  Prenatal diagnosis of sickle cell disease by the technique of PCR.

Authors:  Praneeta J Singh; A C Shrivastava; A V Shrikhande
Journal:  Indian J Hematol Blood Transfus       Date:  2014-07-08       Impact factor: 0.900

Review 4.  From Prenatal to Preimplantation Genetic Diagnosis of β-Thalassemia. Prevention Model in 8748 Cases: 40 Years of Single Center Experience.

Authors:  Giovanni Monni; Cristina Peddes; Ambra Iuculano; Rosa Maria Ibba
Journal:  J Clin Med       Date:  2018-02-20       Impact factor: 4.241

  4 in total

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