Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnancies
Author:
Affiliation:
1. Cytogenetics and Genomics; Quest Diagnostics Nichols Institute; San Juan Capistrano California
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.5375/fullpdf
Reference20 articles.
1. Chromosomal microarray versus karyotyping for prenatal diagnosis;Wapner;N Engl J Med,2012
2. Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens;Shaffer;Prenat Diagn,2008
3. Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies;Shaffer;Prenat Diagn,2012
4. ACMG standards and guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013;South;Genet Med,2013
5. Referral patterns for microarray testing in prenatal diagnosis;Shaffer;Prenat Diagn,2012
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