Article

Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: A retrospective population-based cohort study

2024-04-19

Abstract excerpt

<title>Abstract</title> <p>Background There are no established guidelines for the follow up of infants born after a prenatal diagnosis of a genomic copy number variant (CNV), despite their increased risk of developmental issues. The aims of this study were (i) to determine the perinatal outcomes of fetuses diagnosed with and without a CNV, and (ii) to establish a population-based paediatric cohort for long term...

Topics

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

Identifiers and source

Literature Corpus work: b283727d-aac1-5aed-9292-2010944cb57f
DOI: 10.21203/rs.3.rs-4285240/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: A retrospective population-based cohort studyDOI 10.21203/rs.3.rs-4285240/v1Read

Perinatal outcomes and genomic characteristics of fetal copy number variants: An individual record linkage study of 713 pregnanciesSemantic proximity Read

Childhood outcomes of fetal genomic copy number variants: the prenatal microarray cohort studySemantic proximity Read

Perinatal outcomes of fetuses with pathogenic copy number variants (pCNVs) and confirmed parental inheritance patterns: A retrospective study at a single institutionSemantic proximity Read

Prenatal detection of copy number variants.Semantic proximity Read

Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal servicesSemantic proximity Read

Prenatally detected copy number variants in a national cohort: A postnatal follow‐up studySemantic proximity Read

Array Comparative Genomic Hybridization (aCGH) Results among Patients Referred to Invasive Prenatal Testing after First-Trimester Screening: A Comprehensive Cohort StudySemantic proximity Read

A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective reviewSemantic proximity Read

The predictive value of noninvasive prenatal screening for copy number variations: a cohort study and a systematic meta-analysisSemantic proximity Read

Contribution of de novo and inherited rare CNVs to very preterm birth.Semantic proximity Read

The prenatal diagnosis and clinical outcomes of fetuses with 15q11.2 copy number variants: a case series of 36 patientsSemantic proximity Read

Pregnancy Outcome following Prenatal Diagnosis of Chromosomal Anomaly: A Record Linkage Study of 26,261 PregnanciesSemantic proximity Read