Expanded Carrier Screening
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Obstetrics and Gynaecology
Reference5 articles.
1. Carrier screening in the age of genomic medicine. Committee Opinion No. 690. American College of Obstetricians and Gynecologists;Obstet Gynecol,2017
2. Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine;Edwards;Obstet Gynecol,2015
3. The cystic fibrosis mutation “arms race”: when less is more;Grody;Genet Med,2007
4. Finding middle ground in constructing a clinically useful expanded carrier screening panel;Stevens;Obstet Gynecol,2017
5. An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals;Lazarin;Genet Med,2013
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2. Whole-genome sequencing as a method of prenatal genetic diagnosis: Ethical issues;Clinical Ethics At the Crossroads of Genetic and Reproductive Technologies;2023
3. Couple screening for recessively inherited disorders;Journal of Medical Screening;2022-11-17
4. Decision-making for prenatal genetic screening: how will pregnant women navigate a growing number of aneuploidy and carrier screening options?;BMC Pregnancy and Childbirth;2021-12
5. Women, Children, Families and the Translation of Genomics in Reproductive Medicine;The International Library of Bioethics;2021-11-25
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