Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions
Authors
Keywords
-
Journal
PRENATAL DIAGNOSIS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2018-08-10
DOI
10.1002/pd.5342
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Confined placental mosaicism for 22q11.2 deletion as the etiology for discordant positive NIPT results
- (2017) M. Bunnell et al. PRENATAL DIAGNOSIS
- Mechanisms underlying structural variant formation in genomic disorders
- (2016) Claudia M. B. Carvalho et al. NATURE REVIEWS GENETICS
- Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis
- (2015) Francesca Malvestiti et al. PRENATAL DIAGNOSIS
- Cytogenetic follow-up of chromosomal mosaicism detected in first-trimester prenatal diagnosis
- (2014) Paola Battaglia et al. PRENATAL DIAGNOSIS
- High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power
- (2014) Beatrice Oneda et al. PRENATAL DIAGNOSIS
- Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test
- (2014) Louise Carey et al. PRENATAL DIAGNOSIS
- Confined placental mosaicism: implications for fetal chromosomal analysis using microarray comparative genomic hybridization
- (2013) Evangelia Karampetsou et al. PRENATAL DIAGNOSIS
- Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
- (2012) Ronald J. Wapner et al. NEW ENGLAND JOURNAL OF MEDICINE
- Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies
- (2012) Lisa G. Shaffer et al. PRENATAL DIAGNOSIS
- Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature
- (2012) Amy Breman et al. PRENATAL DIAGNOSIS
- Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases
- (2011) Francesco Fiorentino et al. PRENATAL DIAGNOSIS
- aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis
- (2011) Isabel Filges et al. PRENATAL DIAGNOSIS
- Detection of clinically relevant exonic copy-number changes by array CGH
- (2010) Philip M. Boone et al. HUMAN MUTATION
- Low-level mosaicism of trisomy 14: Phenotypic and molecular characterization
- (2008) Marwan Shinawi et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis
- (2008) X.-Y. Lu et al. PEDIATRICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started