author_facet Claussen, Uwe
Ulmer, Renate
Beinder, Ernst
Voigt, Hans‐Joachim
Claussen, Uwe
Ulmer, Renate
Beinder, Ernst
Voigt, Hans‐Joachim
author Claussen, Uwe
Ulmer, Renate
Beinder, Ernst
Voigt, Hans‐Joachim
spellingShingle Claussen, Uwe
Ulmer, Renate
Beinder, Ernst
Voigt, Hans‐Joachim
Prenatal Diagnosis
Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
Genetics (clinical)
Obstetrics and Gynecology
author_sort claussen, uwe
spelling Claussen, Uwe Ulmer, Renate Beinder, Ernst Voigt, Hans‐Joachim 0197-3851 1097-0223 Wiley Genetics (clinical) Obstetrics and Gynecology http://dx.doi.org/10.1002/pd.1970131203 <jats:title>Abstract</jats:title><jats:p>Rapid karyotyping in the second and third trimesters has important implications for the management of pregnancies at risk. From September 1985 to March 1992, 735 amniotic fluid samples sent to our laboratory for rapid karyotyping from 64 different diagnostic centres of the Federal Republic of Germany were included in a comparative study on harvesting for chromosome analysis using the ‘pipette method’ or the ‘<jats:italic>in situ</jats:italic>’ technique. The average time between preparation of the amniotic fluid and verbal notification of the analysed karyotype was 5·41 days. The ‘pipette method’ needed on average 4·65 days, and the ‘<jats:italic>in situ</jats:italic>’ technique 5·97 days. In comparison with other more invasive techniques available for rapid karyotyping such as cordocentesis and placental biopsy, amniocentesis and subsequent chromosome harvesting using the ‘pipette method’ and/or the ‘<jats:italic>in situ</jats:italic>’ technique proved very useful and efficient. The overall incidence of chromosome aberrations was 15·3 per cent. The high rate of structural chromosome aberrations and uncommon aneuploidies found in our investigation (12 per cent) indicates that for rapid karyotyping in the second and third trimesters, conventional cytogenetic techniques cannot be replaced by faster techniques based on fluorescent <jats:italic>in situ</jats:italic> hybridization on interphase cells in the near future.</jats:p> Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘<i>in situ</i>’ technique for chromosome harvesting Prenatal Diagnosis
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title Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_unstemmed Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_full Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_fullStr Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_full_unstemmed Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_short Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_sort rapid karyotyping in prenatal diagnosis: a comparative study of the ‘pipette method’ and the ‘<i>in situ</i>’ technique for chromosome harvesting
topic Genetics (clinical)
Obstetrics and Gynecology
url http://dx.doi.org/10.1002/pd.1970131203
publishDate 1993
physical 1085-1093
description <jats:title>Abstract</jats:title><jats:p>Rapid karyotyping in the second and third trimesters has important implications for the management of pregnancies at risk. From September 1985 to March 1992, 735 amniotic fluid samples sent to our laboratory for rapid karyotyping from 64 different diagnostic centres of the Federal Republic of Germany were included in a comparative study on harvesting for chromosome analysis using the ‘pipette method’ or the ‘<jats:italic>in situ</jats:italic>’ technique. The average time between preparation of the amniotic fluid and verbal notification of the analysed karyotype was 5·41 days. The ‘pipette method’ needed on average 4·65 days, and the ‘<jats:italic>in situ</jats:italic>’ technique 5·97 days. In comparison with other more invasive techniques available for rapid karyotyping such as cordocentesis and placental biopsy, amniocentesis and subsequent chromosome harvesting using the ‘pipette method’ and/or the ‘<jats:italic>in situ</jats:italic>’ technique proved very useful and efficient. The overall incidence of chromosome aberrations was 15·3 per cent. The high rate of structural chromosome aberrations and uncommon aneuploidies found in our investigation (12 per cent) indicates that for rapid karyotyping in the second and third trimesters, conventional cytogenetic techniques cannot be replaced by faster techniques based on fluorescent <jats:italic>in situ</jats:italic> hybridization on interphase cells in the near future.</jats:p>
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author Claussen, Uwe, Ulmer, Renate, Beinder, Ernst, Voigt, Hans‐Joachim
author_facet Claussen, Uwe, Ulmer, Renate, Beinder, Ernst, Voigt, Hans‐Joachim, Claussen, Uwe, Ulmer, Renate, Beinder, Ernst, Voigt, Hans‐Joachim
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description <jats:title>Abstract</jats:title><jats:p>Rapid karyotyping in the second and third trimesters has important implications for the management of pregnancies at risk. From September 1985 to March 1992, 735 amniotic fluid samples sent to our laboratory for rapid karyotyping from 64 different diagnostic centres of the Federal Republic of Germany were included in a comparative study on harvesting for chromosome analysis using the ‘pipette method’ or the ‘<jats:italic>in situ</jats:italic>’ technique. The average time between preparation of the amniotic fluid and verbal notification of the analysed karyotype was 5·41 days. The ‘pipette method’ needed on average 4·65 days, and the ‘<jats:italic>in situ</jats:italic>’ technique 5·97 days. In comparison with other more invasive techniques available for rapid karyotyping such as cordocentesis and placental biopsy, amniocentesis and subsequent chromosome harvesting using the ‘pipette method’ and/or the ‘<jats:italic>in situ</jats:italic>’ technique proved very useful and efficient. The overall incidence of chromosome aberrations was 15·3 per cent. The high rate of structural chromosome aberrations and uncommon aneuploidies found in our investigation (12 per cent) indicates that for rapid karyotyping in the second and third trimesters, conventional cytogenetic techniques cannot be replaced by faster techniques based on fluorescent <jats:italic>in situ</jats:italic> hybridization on interphase cells in the near future.</jats:p>
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spelling Claussen, Uwe Ulmer, Renate Beinder, Ernst Voigt, Hans‐Joachim 0197-3851 1097-0223 Wiley Genetics (clinical) Obstetrics and Gynecology http://dx.doi.org/10.1002/pd.1970131203 <jats:title>Abstract</jats:title><jats:p>Rapid karyotyping in the second and third trimesters has important implications for the management of pregnancies at risk. From September 1985 to March 1992, 735 amniotic fluid samples sent to our laboratory for rapid karyotyping from 64 different diagnostic centres of the Federal Republic of Germany were included in a comparative study on harvesting for chromosome analysis using the ‘pipette method’ or the ‘<jats:italic>in situ</jats:italic>’ technique. The average time between preparation of the amniotic fluid and verbal notification of the analysed karyotype was 5·41 days. The ‘pipette method’ needed on average 4·65 days, and the ‘<jats:italic>in situ</jats:italic>’ technique 5·97 days. In comparison with other more invasive techniques available for rapid karyotyping such as cordocentesis and placental biopsy, amniocentesis and subsequent chromosome harvesting using the ‘pipette method’ and/or the ‘<jats:italic>in situ</jats:italic>’ technique proved very useful and efficient. The overall incidence of chromosome aberrations was 15·3 per cent. The high rate of structural chromosome aberrations and uncommon aneuploidies found in our investigation (12 per cent) indicates that for rapid karyotyping in the second and third trimesters, conventional cytogenetic techniques cannot be replaced by faster techniques based on fluorescent <jats:italic>in situ</jats:italic> hybridization on interphase cells in the near future.</jats:p> Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘<i>in situ</i>’ technique for chromosome harvesting Prenatal Diagnosis
spellingShingle Claussen, Uwe, Ulmer, Renate, Beinder, Ernst, Voigt, Hans‐Joachim, Prenatal Diagnosis, Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting, Genetics (clinical), Obstetrics and Gynecology
title Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_full Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_fullStr Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_full_unstemmed Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_short Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
title_sort rapid karyotyping in prenatal diagnosis: a comparative study of the ‘pipette method’ and the ‘<i>in situ</i>’ technique for chromosome harvesting
title_unstemmed Rapid karyotyping in prenatal diagnosis: A comparative study of the ‘pipette method’ and the ‘in situ’ technique for chromosome harvesting
topic Genetics (clinical), Obstetrics and Gynecology
url http://dx.doi.org/10.1002/pd.1970131203