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 isolated clubfoot increases the risk for clinically significant exome sequencing results

3 Nov 2022

Abstract excerpt

OBJECTIVE: To examine the diagnostic yield of exome sequencing (ES) in singleton pregnancies with isolated fetal clubfoot. METHODS: Clinical data from singleton pregnancies with a sonographic diagnosis of isolated clubfoot and ES results between 2018 and 2021 were retrospectively obtained from a single referral medical center. The recorded data include maternal age, gestational age at sonographic diagnosis, the...

Read the complete abstract on PubMed

Topics

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

Share to Neurogenetic and Muscular Disorders Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36326072
DOI: 10.1002/pd.6259

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

Prenatal isolated clubfoot increases the risk for clinically significant exome sequencing resultsPMID 36326072Read ↗

Genetic analysis in fetuses with isolated clubfoot: diagnostic insights and added valueSemantic proximity Read ↗

Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysisSemantic proximity Read ↗

Utility of whole exome sequencing in the evaluation of isolated fetal growth restriction in normal chromosomal microarray analysisSemantic proximity Read ↗

Genetic Analysis of Isolated Fetal Growth RestrictionSemantic proximity Read ↗

Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion.Semantic proximity Read ↗

Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisSemantic proximity Read ↗

RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis.Semantic proximity Read ↗

Genome sequencing in a cohort of 32 fetuses with genetic skeletal disordersSemantic proximity Read ↗

Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese casesSemantic proximity Read ↗

Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetusesSemantic proximity Read ↗

Inherited variants in autosomal dominant disease genes are a significant cause of fetal structural anomalies.Semantic proximity Read ↗

Prenatal exome sequencing for the morphologically normal fetus: Should we be doing it?Semantic proximity Read ↗

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