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Prenatal Screening and Diagnostics |
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Information obtained from prenatal testing can assist in pregnancy management, indicate the presence of a congenital abnormality or genetic disorder, predict a complicated delivery, and determin potential risks in future pregnancies.
Prenatal testing is generally performed on amniocytes (cells in the amniotic fluid) or on the amniotic fluid (AF). Certain testing can also be performed on a percutaneous umbilical cord blood sample (PUBS) or on a chorionic villus sample (CVS). Our comprehensive prental screening and prenatal diagnostic test menu includes routine screening and genetic, karyotype and fluorescence in situ hybridization (FISH) testing to identify microdeletion syndromes.
Prenatal Screening
HPV testing and HPV genotyping
Maternal serum screening and quad screen
 Obstetric clinical testing panel test information and specimen requirements »
Prenatal Diagnostics & High-Risk Obstetrics
Alpha-fetoprotein testing
Constitutional FISH and prenatal diagnostics
Indications for chromosome analysis
Inherited genetic disorders & cystic fibrosis
Thrombotic risk assessment
Fertility testing
Genetic counseling
Our Testing Resources
 Prenatal testing services
 Cytogenetics services
Cytogenetics tissue requirements
Prenatal diagnostics
Prenatal diagnostic chart
Laboratory Services in One Location
Anatomic Pathology | Immunohistochemistry | Immunomagnetic Cell Capture (CellSearch)
Flow Cytometry | Cytogenetics | Fluorescence in situ hybridization (FISH) | Molecular Diagnostics
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