Prenatal Molecular Diagnostics
Much research is being done in foetal whole exome sequencing and is beginning to play a large role in miscarriage testing. With all this research and screening, clinicians and genetic counsellors need to keep abreast of these changes and guidelines in order to effectively care for patients.
The genetic cause of foetal abnormalities detected on ultrasound imaging and in high-risk families can be significantly identified and improved in Foetal diagnostic exome sequencing. Testing based on isolation of foetal cells from maternal blood would provide an attractive alternative to testing of cell-free DNA. An updated implementation of these different approaches will make lively discussion and insight into this field and is headed ways for researchers, test providers, clinicians and clinics to take these developments into consideration.
- Advances in Prenatal Molecular Diagnostics
- Cell-free DNA screening
- Cell-based DNA testing
- Biomarkers for preeclampsia and pre-term birth
- Prenatal and Reproductive Diagnostics
- Non-Invasive Prenatal Diagnosis
Related Conference of Prenatal Molecular Diagnostics
Prenatal Molecular Diagnostics Conference Speakers