Article

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

2025-11-10

Abstract excerpt

<title>Abstract</title> <p> <bold>Background</bold> Advances in genomic technologies, including chromosomal microarray (CMA) and whole-exome sequencing (WES), have provided tools to explore genetic factors of cleft lip and/or palate (CL/P). However, further investigation is warranted to identify the spectrum of phenotype and genetic variants in both syndromic and non-syndromic CL/P. <bold>Methods</bold> Fifty...

Topics

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

Identifiers and source

Literature Corpus work: fce2c649-cfa2-53bb-b2dc-2d37f34ed63b
DOI: 10.21203/rs.3.rs-7069278/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Spectrum of phenotype and genetic variants in a Suzhou cohort of fetuses with cleft lip and/or palateDOI 10.21203/rs.3.rs-7069278/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

Identification of susceptibility genes in non-syndromic cleft lip with or without cleft palate using whole-exome sequencing.Semantic proximity Read

Exome Sequencing Studies in Syndromic Patients With Cleft Lip and/or Palate: Systematic Review.Semantic proximity Read

Prenatal diagnosis of fetuses with ultrasound anomalies by whole-exome sequencing in Luoyang city, ChinaSemantic proximity Read

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.Semantic proximity Read

Genetics of cleft lip and cleft palate.Semantic proximity Read

Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesSemantic proximity Read

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

[Progress in genetic epidemiology of non-syndromic cleft palate only].Semantic proximity Read

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial cleftingSemantic proximity Read

Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing StudySemantic proximity Read