Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA

28 Jan 2019

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cancer Genomics and Diagnostics
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 30692697
DOI: 10.1038/s41591-018-0334-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNAPMID 30692697Read ↗

Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNASemantic proximity Read ↗

Non-invasive prenatal diagnosis (NIPD): current and emerging technologiesSemantic proximity Read ↗

Noninvasive fetal genome sequencing: a primerSemantic proximity Read ↗

Non-invasive prenatal diagnosis (NIPD): how analysis of cell-free DNA in maternal plasma has changed prenatal diagnosis for monogenic disordersSemantic proximity Read ↗

Advances in Prenatal Cell‐Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical ImplementationSemantic proximity Read ↗

Non-invasive prenatal testing using cell-free fetal DNA in maternal circulationSemantic proximity Read ↗

Noninvasive Whole-Genome Sequencing of a Human FetusSemantic proximity Read ↗

cfDNA screening and diagnosis of monogenic disorders – where are we heading?Semantic proximity Read ↗

Non-invasive prenatal diagnosis of single-gene disorders from maternal bloodSemantic proximity Read ↗

Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma.Semantic proximity Read ↗

Non-invasive prenatal testing using massively parallel sequencing of maternal plasma DNA: from molecular karyotyping to fetal whole-genome sequencingSemantic proximity Read ↗

Non-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.