Cell-free fetal DNA screening for detection of microdeletion syndromes: a cost-effectiveness analysis
Author:
Affiliation:
1. Department of Obstetrics and Gynecology, Oregon Health & Sciences University, Portland, OR, USA
2. Department of Obstetrics, Gynecology, and Reproductive Sciences, Univeristy of California San Francisco, San Francisco, CA, USA
Funder
National Institutes of Health
Fetal Health Foundation
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2019.1647161
Reference42 articles.
1. Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes
2. Clinical outcome of subchromosomal events detected by whole‐genome noninvasive prenatal testing
3. The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature
4. Prenatal diagnosis by chromosomal microarray analysis
5. Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome
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