Article
Copy-number changes in prenatal diagnosis.
Expert review of molecular diagnostics - 1 Jul 2011
Strassberg Melissa, Fruhman Gary, Van den Veyver Ignatia B
Abstract excerpt
Until recently, the prenatal detection of genetic disease was available to only a subset of the pregnant population deemed to be at an increased risk for chromosomal abnormalities or, more rarely, other genetic disorders, based on family history, multiple-marker screening or ultrasound findings. Guided by recent data that indicate that screening for Down syndrome has improved and that risks of invasive procedures...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.