Back to search

Article

Nonivasive prenatal diagnosis of single-gene disorders using droplet digital PCR

2017-08-23

Abstract excerpt

<h4>Background</h4> Prenatal diagnosis in pregnancies at risk of single-gene disorders is currently performed using invasive methods such as chorionic villus sampling and amniocentesis. This is in contrast with screening for common aneuploidies, for which noninvasive methods with a single maternal blood sample have become standard clinical practice. <h4>Methods</h4> We developed a protocol for noninvasive prenat...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
36a92f19-079d-50d8-9805-f2f3f960909d
DOI
10.1101/179804
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Nonivasive prenatal diagnosis of single-gene disorders using droplet digital PCRDOI 10.1101/179804
Select a neighboring publication to make it the new centre.