Cargando…

Chromosome microarray analysis combined with karyotype analysis is a powerful tool for the detection in pregnant women with high-risk indicators

BACKGROUND: Karyotype analysis and fluorescence in situ hybridization (FISH) are commonly used for prenatal diagnosis, however they have many disadvantages. Chromosome microarray analysis (CMA) has the potential to overcome these disadvantages. This study aimed to evaluate the clinical value of CMA...

Descripción completa

Detalles Bibliográficos
Autores principales:	Qian, Guanhua, Cai, Liuyun, Yao, Hong, Dong, Xiaojing
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2023
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10638706/ https://www.ncbi.nlm.nih.gov/pubmed/37951870 http://dx.doi.org/10.1186/s12884-023-06052-z

Ejemplares similares

Chromosomal mosaicism detected by karyotyping and chromosomal microarray analysis in prenatal diagnosis
por: Zhang, Yi, et al.
Publicado: (2020)

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

Chromosomal microarray analysis vs. karyotyping for fetal ventriculomegaly: a meta-analysis
por: Sun, Yan, et al.
Publicado: (2022)

Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency
por: Cicatiello, Rita, et al.
Publicado: (2019)

The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis
por: Hao, MengZhe, et al.
Publicado: (2020)

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

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
por: Shi, Xiaomei, et al.
Publicado: (2021)

Karyotyping and Chromosomal Microarray Analysis in Women Requesting Amniocentesis for Isolated Sonographic Soft Markers or Advanced Maternal Age
por: Tzela, Panagiota, et al.
Publicado: (2021)

Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies
por: Wang, Jin, et al.
Publicado: (2022)

Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis
por: Guo, Huan, et al.
Publicado: (2023)

Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results
por: Kang, Han, et al.
Publicado: (2022)

Chromosome Analysis Using Spectral Karyotyping (SKY)
por: Imataka, George, et al.
Publicado: (2011)

A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant Women
por: Jiang, Minmin, et al.
Publicado: (2022)

Epidemiology of fetal cerebral ventriculomegaly and evaluation of chromosomal microarray analysis versus karyotyping for prenatal diagnosis in a Chinese hospital
por: Yi, Jun-Ling, et al.
Publicado: (2019)

Clinical Application of Chromosomal Microarray Analysis in Pregnant Women with Advanced Maternal Age and Fetuses with Ultrasonographic Soft Markers
por: Hu, Zhu-Ming, et al.
Publicado: (2021)

Effectiveness of non-invasive chromosomal screening for normal karyotype and chromosomal rearrangements
por: Sun, Bo-lan, et al.
Publicado: (2023)

Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review
por: Tse, Kai Yeung, et al.
Publicado: (2023)

Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women
por: Younesi, Sarang, et al.
Publicado: (2021)

Retracted: A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant Women
por: and Alternative Medicine, Evidence-Based Complementary
Publicado: (2023)

Molecular microdeletion analysis of infertile men with karyotypic Y chromosome abnormalities
por: Pan, Yuan, et al.
Publicado: (2017)

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

Study on the application value of BACs-on-Beads technology combined with chromosome karyotype analysis in prenatal diagnosis
por: Chen, Lin, et al.
Publicado: (2022)

Chromosomal rearrangements and karyotype evolution in carnivores revealed by chromosome painting
por: Nie, W, et al.
Publicado: (2012)

Comparative karyotype analysis and chromosome evolution in the genus Aplastodiscus (Cophomantini, Hylinae, Hylidae)
por: Gruber, Simone Lilian, et al.
Publicado: (2012)

Cell culture-based karyotyping of orectolobiform sharks for chromosome-scale genome analysis
por: Uno, Yoshinobu, et al.
Publicado: (2020)

Analysis of Paralogons, Origin of the Vertebrate Karyotype, and Ancient Chromosomes Retained in Extant Species
por: Lamb, Trevor D
Publicado: (2021)

Protein and Chemical Microarrays—Powerful Tools for Proteomics
por: Xu, Qingchai, et al.
Publicado: (2003)

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)

Karyotypic polymorphism of the zebra finch Z chromosome
por: Itoh, Yuichiro, et al.
Publicado: (2011)

Updating the maize karyotype by chromosome DNA sizing
por: Silva, Jéssica Coutinho, et al.
Publicado: (2018)

Loss of X Chromosome Inactivation in Androgenetic Complete Hydatidiform Moles With 46, XX Karyotype
por: Chen, Xiaojing, et al.
Publicado: (2021)

Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype
por: Khan, Abdul Waheed, et al.
Publicado: (2020)

Insights into the karyotype and genome evolution of haplogyne spiders indicate a polyploid origin of lineage with holokinetic chromosomes
por: Král, Jiří, et al.
Publicado: (2019)

Application of chromosomal microarray analysis in products of miscarriage
por: Zhu, Xiangyu, et al.
Publicado: (2018)

Application of chromosome microarray analysis in prenatal diagnosis
por: Xia, Mingjing, et al.
Publicado: (2020)

Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype
por: Pratte-Santos, Rodrigo, et al.
Publicado: (2016)

Analysis of chromosome karyotype and genome size in echiuran Urechisunicinctus Drasche, 1880 (Polychaeta, Urechidae)
por: Qin, Zhenkui, et al.
Publicado: (2019)

Chromosomal copy number analysis of products of conception by conventional karyotyping and next‐generation sequencing
por: Tamura, Yuki, et al.
Publicado: (2020)

CytoGPS: a web-enabled karyotype analysis tool for cytogenetics
por: Abrams, Zachary B, et al.
Publicado: (2019)

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

Cannot write session to /tmp/vufind_sessions/sess_5oq5f4ps9ojrkd8460hjt5ch93