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

Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges

18 May 2017

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 Genomic variations and chromosomal abnormalities
Share to Genomics and Rare Diseases
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 28518170
DOI: 10.1038/gim.2017.33

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 20 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesPMID 28518170Read ↗

Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A ReviewSemantic proximity Read ↗

Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomaliesSemantic proximity Read ↗

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort studySemantic proximity Read ↗

8: Whole exome sequencing in the evaluation of fetal structural anomalies: A prospective study of sequential patientsSemantic proximity Read ↗

An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceSemantic proximity Read ↗

Prenatal exome and genome sequencing for fetal structural abnormalitiesSemantic proximity Read ↗

Update on the use of exome sequencing in the diagnosis of fetal abnormalitiesSemantic proximity Read ↗

Prenatal next-generation sequencing in the fetus with congenital malformations: how can we improve clinical utility?Semantic proximity Read ↗

Considerations for whole exome sequencing unique to prenatal careSemantic proximity Read ↗

The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

Exome Sequencing in Fetuses with Structural MalformationsSemantic proximity Read ↗

Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital AnomaliesSemantic proximity Read ↗

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