AbstractFetal cells occur in maternal blood in a substantial proportion of normal pregnancies. Several different approaches have been used to detect and enrich these cells for non-invasive prenatal diagnosis. However, before these fetal cells can routinely be used for prenatal diagnosis, perfectly reproducible procedures for detection and enrichment need to be established. We found that these fetal cells express high intracellular levels of the DNA precursor pathway enzyme thymidine kinase. Since normal adult peripheral blood cells do not exhibit any thymidine kinase activity, this enzyme is a potent new marker to detect and enrich fetal cells from maternal blood. We further describe the first successful application of a cytofluorometric th...
In 1997, Prof. Dennis Lo discovered the presence of cell-free fetal DNA (cffDNA) in the maternal pla...
Prenatal diagnosis plays a crucial role in clinical genetics. Non-invasive prenatal diagnosis using ...
The discovery of circulating cell-free fetal DNA in maternal plasma/serum, in 1997, and the demonstr...
AbstractFetal cells occur in maternal blood in a substantial proportion of normal pregnancies. Sever...
Fetal cells that circulate in maternal peripheral blood during pregnancy offer a potential source of...
We report the detection of fetal cells in the maternal circulation by enzymatic amplification of a s...
In this study we evaluated the performance of a system for the enrichment, identification and analys...
The isolation and analysis of fetal cells from maternal blood would allow non-invasive prenatal gene...
Fetal cells circulate in maternal blood and are considered a suitable means by which to detect fetal...
Prenatal diagnosis of genetic disorders has traditionally relied on invasive procedures such as amni...
Strategies for genetic prenatal diagnosis on fetal cells in the maternal circulation have been limit...
OBJECTIVE: Fetal cells circulate in the maternal blood during early pregnancy. Because these cells a...
One potential noninvasive approach for antenatal diag-nosis is the use of fetal cells in maternal ci...
Currently prenatal diagnosis relies on invasive procedures such as chorion villus sampling (CVS) or ...
Delaying childbirth increases the proportion of advanced maternal age pregnancies. This increases th...
In 1997, Prof. Dennis Lo discovered the presence of cell-free fetal DNA (cffDNA) in the maternal pla...
Prenatal diagnosis plays a crucial role in clinical genetics. Non-invasive prenatal diagnosis using ...
The discovery of circulating cell-free fetal DNA in maternal plasma/serum, in 1997, and the demonstr...
AbstractFetal cells occur in maternal blood in a substantial proportion of normal pregnancies. Sever...
Fetal cells that circulate in maternal peripheral blood during pregnancy offer a potential source of...
We report the detection of fetal cells in the maternal circulation by enzymatic amplification of a s...
In this study we evaluated the performance of a system for the enrichment, identification and analys...
The isolation and analysis of fetal cells from maternal blood would allow non-invasive prenatal gene...
Fetal cells circulate in maternal blood and are considered a suitable means by which to detect fetal...
Prenatal diagnosis of genetic disorders has traditionally relied on invasive procedures such as amni...
Strategies for genetic prenatal diagnosis on fetal cells in the maternal circulation have been limit...
OBJECTIVE: Fetal cells circulate in the maternal blood during early pregnancy. Because these cells a...
One potential noninvasive approach for antenatal diag-nosis is the use of fetal cells in maternal ci...
Currently prenatal diagnosis relies on invasive procedures such as chorion villus sampling (CVS) or ...
Delaying childbirth increases the proportion of advanced maternal age pregnancies. This increases th...
In 1997, Prof. Dennis Lo discovered the presence of cell-free fetal DNA (cffDNA) in the maternal pla...
Prenatal diagnosis plays a crucial role in clinical genetics. Non-invasive prenatal diagnosis using ...
The discovery of circulating cell-free fetal DNA in maternal plasma/serum, in 1997, and the demonstr...