Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value

Am J Obstet Gynecol. 2015 Aug;213(2):254-5. doi: 10.1016/j.ajog.2015.05.028. Epub 2015 May 15.

Authors

Susan J Gross¹, Allison Ryan¹, Peter Benn²

Affiliations

¹ Natera Inc, 201 Industrial Rd., San Carlos, CA 94070.
² Division of Human Genetics, Department of Genetics and Genome Sciences, University of Connecticut Health Center, 236 Farmington Ave., Farmington, CT 06030-3808. Electronic address: benn@uchc.edu.

PMID: 25986033
DOI: 10.1016/j.ajog.2015.05.028

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Chromosome Deletion*
Chromosome Disorders / diagnosis*
Female
Genetic Testing / methods*
Humans
Maternal Serum Screening Tests*
Polymorphism, Single Nucleotide*
Pregnancy