Parental perceptions of prenatal whole exome sequencing (PPPWES) study

Author:

Wou Karen1ORCID,Weitz Talia2,McCormack Clare3,Wynn Julia1,Spiegel Erica4,Giordano Jessica4,Wapner Ronald J.4,Chung Wendy K.15ORCID

Affiliation:

1. Department of Pediatrics, Division of Clinical Genetics; Columbia University; New York NY USA

2. College of Physicians and Surgeons; Columbia University; New York NY USA

3. Department of Psychiatry, Division of Behavioral Medicine; Columbia University; New York NY USA

4. Department of Obstetrics and Gynecology, Division of Reproductive Genetics; Columbia University; New York NY USA

5. Department of Pediatrics, Division of Molecular Genetics, and Department of Medicine; Columbia University; New York NY USA

Funder

Institute for Genomic Medicine (IGM)

National Institute of Diabetes and Digestive and Kidney Diseases

National Human Genome Research Institute

National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference25 articles.

1. Update on overall prevalence of major birth defects-Atlanta, Georgia, 1978-2005;MMWR Morb Mortal Wkly Rep,2008

2. Infant mortality statistics from the 2013 period linked birth/infant death data set;Mathews;Natl Vital Stat Rep,2015

3. Monitoring the prenatal detection of structural fetal congenital anomalies in England and Wales: register-based study;Boyd;J Med Screen,2011

4. Epidemiology of multiple congenital anomalies in Europe: a EUROCAT population-based registry study;Calzolari;Birth Defects Res A Clin Mol Teratol,2014

5. Chromosomal microarray versus karyotyping for prenatal diagnosis;Wapner;N Engl J Med,2012

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