Article

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center

2024-01-15

Abstract excerpt

<title>Abstract</title> <p><bold>Backgroud:</bold> A systematic analysis was conducted to investigate the molecular etiology of fetal cleft lip and/or palate (CL/CP) and the association between various types of CL/CP and copy number variations (CNVs), as well as their impact on birth outcomes. <bold>Methods:</bold>In this retrospective study, a cohort of pregnancies diagnosed with fetal CL/CP was enrolled and com...

Topics

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

Identifiers and source

Literature Corpus work: c9965c7f-7d25-5deb-8370-1a94e2d430fa
DOI: 10.21203/rs.3.rs-3812609/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary centerDOI 10.21203/rs.3.rs-3812609/v1Read

The clinical utility of genetic technologies in prenatally diagnosed cleft lip and or palate – a cohort studySemantic proximity Read

Prenatal diagnosis of cleft lip and palate: a study of clinical utilitySemantic proximity Read

Spectrum of phenotype and genetic variants in a Suzhou cohort of fetuses with cleft lip and/or palateSemantic proximity Read

Prenatal diagnosis of cleft lip and cleft lip palate – a case seriesSemantic proximity Read

Understanding Pathogenic Detection Rates of CNVs in Prenatal Diagnosis: Insights from a Cohort StudySemantic proximity Read

Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohortSemantic proximity Read

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

Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palateSemantic proximity Read

Prenatal genetic evaluation and outcomes in pregnancies with first-occurrence typical orofacial cleftsSemantic proximity Read

Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.Semantic proximity Read

Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal ageSemantic proximity Read

A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated?Semantic proximity Read