Cargando…

Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China

Numerous studies have evaluated the use of single nucleotide polymorphism array (SNP-array) in prenatal diagnostics, but very few have evaluated its application under different risk conditions. Here, SNP-array was used for the retrospective analysis of 8386 pregnancies and the cases were categorized...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cai, Meiying, Lin, Na, Guo, Nan, Su, Linjuan, Wu, Xiaoqing, Xie, Xiaorui, Li, Ying, He, Shuqiong, Fu, Xianguo, Xu, Liangpu, Huang, Hailong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160013/ https://www.ncbi.nlm.nih.gov/pubmed/37142625 http://dx.doi.org/10.1038/s41598-023-33668-0

Ejemplares similares

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
por: Cai, Meiying, et al.
Publicado: (2020)

Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes
por: Cai, Meiying, et al.
Publicado: (2021)

Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities
por: Xie, Xiaorui, et al.
Publicado: (2021)

Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome
por: Cai, Meiying, et al.
Publicado: (2018)

Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities
por: Cai, Meiying, et al.
Publicado: (2021)

Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays
por: Cai, Meiying, et al.
Publicado: (2019)

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
por: Wu, Xiaoqing, et al.
Publicado: (2019)

Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center
por: Cai, Meiying, et al.
Publicado: (2022)

Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing
por: Wu, Xiaoqing, et al.
Publicado: (2021)

Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis
por: Xie, Xiaorui, et al.
Publicado: (2023)

Prenatal diagnosis of Pallister‐Killian syndrome and literature review
por: Wu, Xiaoqing, et al.
Publicado: (2021)

Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith–Magenis and Potocki–Lupski Syndromes in Fetuses
por: Cai, Meiying, et al.
Publicado: (2021)

Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease
por: Xue, Huili, et al.
Publicado: (2021)

Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China
por: Zheng, Lin, et al.
Publicado: (2021)

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype
por: Wu, Xiaoqing, et al.
Publicado: (2020)

Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes
por: Cai, Meiying, et al.
Publicado: (2020)

SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis
por: Huang, Hailong, et al.
Publicado: (2021)

Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities
por: Su, Linjuan, et al.
Publicado: (2021)

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
por: Su, Linjuan, et al.
Publicado: (2019)

Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis
por: Cai, Meiying, et al.
Publicado: (2023)

Copy number variations associated with fetal congenital kidney malformations
por: Cai, Meiying, et al.
Publicado: (2020)

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
por: Wu, Xiaoqing, et al.
Publicado: (2019)

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
por: Cai, Meiying, et al.
Publicado: (2018)

Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios
por: Wu, Xiaoqing, et al.
Publicado: (2022)

Retrospective analysis of the sex chromosomal copy number variations in 186 fetuses using single nucleotide polymorphism arrays
por: Wang, Haiwei, et al.
Publicado: (2022)

Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome
por: Cai, Meiying, et al.
Publicado: (2022)

Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women
por: Cai, Meiying, et al.
Publicado: (2021)

Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays
por: Xue, Huili, et al.
Publicado: (2021)

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study
por: Huang, Hailong, et al.
Publicado: (2021)

Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities
por: Guo, Nan, et al.
Publicado: (2022)

Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience
por: Huang, Hailong, et al.
Publicado: (2021)

Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience
por: Liang, Bin, et al.
Publicado: (2022)

Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
por: Wu, Xiaoqing, et al.
Publicado: (2021)

Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort Study
por: Cai, Meiying, et al.
Publicado: (2022)

Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience
por: Wu, Xiaoqing, et al.
Publicado: (2023)

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study
por: Cai, Meiying, et al.
Publicado: (2022)

Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies
por: Cai, Meiying, et al.
Publicado: (2021)

Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array
por: Zhou, Lili, et al.
Publicado: (2021)

Comprehensive Assessment of Fetal Bilateral Ventriculomegaly Based on Genetic Disorders, Cytomegalovirus Infection, Extra Prenatal Imaging and Pregnancy Outcomes in a Tertiary Referral Center
por: Guo, Danhua, et al.
Publicado: (2021)

Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism
por: Zhang, Min, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_9fn5lc1ta48l9i9kfbs8tpisto