Cargando…

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies

OBJECTIVE: To describe the diagnostic performance of array comparative genomic hybridization (aCGH) as a potential first line diagnostic method in first trimester high risk pregnancies. METHOD: In a retrospective study we performed aCGH using a targeted array BAC platform (Constitutional Chip® 4.0,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Filges, Isabel, Kang, Anjeung, Klug, Vanessa, Wenzel, Friedel, Heinimann, Karl, Tercanli, Sevgi, Miny, Peter
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462716/ https://www.ncbi.nlm.nih.gov/pubmed/22979998 http://dx.doi.org/10.1186/1755-8166-5-38

Ejemplares similares

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?
por: Miny, Peter, et al.
Publicado: (2013)

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries
por: Meier, Nicole, et al.
Publicado: (2019)

Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly
por: Meier, Nicole, et al.
Publicado: (2020)

Comparison of Efficiencies of Non-invasive Prenatal Testing, Karyotyping, and Chromosomal Micro-Array for Diagnosing Fetal Chromosomal Anomalies in the Second and Third Trimesters
por: Zhu, Yiyang, et al.
Publicado: (2019)

Association between chromosome abnormities and prenatal diagnosis indicators screening in the second trimester of pregnancy
por: Pan, Ci, et al.
Publicado: (2023)

Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?
por: Hahn, Sinuhe, et al.
Publicado: (2011)

Prenatal Diagnosis of Small Supernumerary Marker Chromosome 10 by Array-Based Comparative Genomic Hybridization and Microdissected Chromosome Sequencing
por: Lebedev, Igor N., et al.
Publicado: (2021)

Frequency and clinical significance of chromosomal inversions prenatally diagnosed by second trimester amniocentesis
por: Chien, Chih-Wei, et al.
Publicado: (2022)

Prenatal diagnosis and pregnancy outcome of major structural anomalies detectable in the first trimester: A population‐based cohort study in the Netherlands
por: Bardi, Francesca, et al.
Publicado: (2022)

How to do a second trimester anomaly scan
por: Carmen Prodan, Natalia, et al.
Publicado: (2022)

Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
por: Anh, Do Duy, et al.
Publicado: (2019)

Pregnancy Outcome following Prenatal Diagnosis of Chromosomal Anomaly: A Record Linkage Study of 26,261 Pregnancies
por: Jacobs, Myrthe, et al.
Publicado: (2016)

Sociodemographic Differences in Prenatal Diagnosis of Chromosomal Anomalies: A Population-Based Study
por: Santoro, Michele, et al.
Publicado: (2021)

Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic Hybridization
por: Cignini, Pietro, et al.
Publicado: (2011)

Genetic Diagnosis of Chromosomal Congenital Anomalies in Albanian Pediatric Patients by Array CGH
por: Babameto-Laku, Anila, et al.
Publicado: (2017)

Prenatal diagnosis: the clinical usefulness of array comparative genomic hybridization
por: Freitas, Marta, et al.
Publicado: (2018)

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis
por: Sun, Lijuan, et al.
Publicado: (2015)

Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy
por: Kolarski, Milenko, et al.
Publicado: (2017)

Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies
por: Basaran, Seher, et al.
Publicado: (2022)

Efficacy of Systematic Early-Second-Trimester Ultrasound Screening for Facial Anomalies: A Comparison between Prenatal Ultrasound and Postmortem Findings
por: Lamanna, Bruno, et al.
Publicado: (2023)

Prenatal diagnosis of congenital anomalies
por: Todros, T, et al.
Publicado: (2001)

Application of a target array Comparative Genomic Hybridization to prenatal diagnosis
por: Park, Ji Hyeon, et al.
Publicado: (2010)

Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities
por: Kowalczyk, Katarzyna, et al.
Publicado: (2021)

Evaluation of prenatal central nervous system anomalies: obstetric management, fetal outcomes and chromosome abnormalities
por: Tan, Ann Gee, et al.
Publicado: (2022)

Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series
por: Wen, Jiadi, et al.
Publicado: (2019)

Prenatal diagnosis and pregnancy outcome analysis of thickened nuchal fold in the second trimester
por: Li, Lushan, et al.
Publicado: (2018)

Normograms in Prenatal Life of Stomach and Urinary Bladder in the Second and Third Trimesters of Pregnancy
por: Witkowski, Sławomir, et al.
Publicado: (2022)

First Trimester Ultrasound in Prenatal Diagnosis—Part of the Turning Pyramid of Prenatal Care
por: Neiger, Ran
Publicado: (2014)

Array comparative genomic hybridization analysis of products of conception in recurrent pregnancy loss for specific anomalies detected by USG
por: Gajjar, Kinjal, et al.
Publicado: (2023)

Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)
por: Plasilova, Martina, et al.
Publicado: (2011)

Screening for chromosomal abnormalities using combined test in the first trimester of pregnancy
por: Park, Soo Yeon, et al.
Publicado: (2016)

The Relationship between Screening Markers in the First Trimester of Pregnancy and Chromosome Aberrations
por: Mirsafaie, Maryam, et al.
Publicado: (2022)

A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics
por: Yin, Aihua, et al.
Publicado: (2014)

Prenatal Diagnosis of Adrenal Neuroblastoma – Differential Diagnosis of Suprarenal Masses in the Third Trimester of Pregnancy
por: Psarris, Alexandros, et al.
Publicado: (2019)

Prenatal Echo-Sonographic Parameters in Fetuses Wrapped with the Umbilical Cord in the Third Trimester of Pregnancy
por: Murlewska, Julia, et al.
Publicado: (2023)

New Tools for Embryo Selection: Comprehensive Chromosome Screening by Array Comparative Genomic Hybridization
por: Rodrigo, Lorena, et al.
Publicado: (2014)

Quantitative Proteomics Analysis of Maternal Plasma in Down Syndrome Pregnancies Using Isobaric Tagging Reagent (iTRAQ)
por: Kolla, Varaprasad, et al.
Publicado: (2010)

Clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies
por: Beulen, L., et al.
Publicado: (2017)

Second‐trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray
por: Drozniewska, Malgorzata, et al.
Publicado: (2020)

Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism
por: Ma, Na, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_df96e169i4a28d3gekuc3hpmpp