Literature DB >> 3222216

Prenatal diagnosis with biotinylated chromosome specific probes.

B Guyot1, A Bazin, Y Sole, C Julien, F Daffos, F Forestier.   

Abstract

We have used a Y-chromosome specific DNA probe in a controlled study to determine the presence of Y-chromosome material and to detect numerical abnormalities in uncultured amniotic fluid cells by fluorescent hybridization. Using this non-radioactive method, we correctly predicted fetal sex within 48 h in all but 3 of 54 cases and identified an XYY syndrome. The technique was previously tested with no false-positive or false-negative results on cultured interphase or metaphase nuclei of fetal fibroblasts and adult T-lymphocytes. Fluorescent in situ hybridization was applied to long-term fixed cytogenetic preparations up to 44 months old and was shown to be reliable.

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Year:  1988        PMID: 3222216     DOI: 10.1002/pd.1970080703

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report.

Authors:  T Bryndorf; B Christensen; J Philip; W Hansen; K Yokobata; N Bui; C Gaiser
Journal:  BMJ       Date:  1992-06-13

Review 2.  Interphase cytogenetics.

Authors:  C S Herrington; J O McGee
Journal:  Neurochem Res       Date:  1990-04       Impact factor: 3.996

3.  Maternal cell contamination in amniotic fluid samples as a consequence of the sampling technique.

Authors:  S Nuss; D Brebaum; C Grond-Ginsbach
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

  3 in total

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