Committee Opinion No. 690: Carrier Screening in the Age of Genomic Medicine
Author:
- Committee on GeneticsCGCommittee on Genetics
- 1 March 2017
- journal article
- practice guideline
- Published by Wolters Kluwer Health in Obstetrics & Gynecology
- Vol. 129 (3) , e35-e40
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Committee Opinion No. 691: Carrier Screening for Genetic ConditionsObstetrics & Gynecology, 2017
- Where to Draw the Boundaries for Prenatal Carrier ScreeningJAMA, 2016
- Modeled Fetal Risk of Genetic Diseases Identified by Expanded Carrier ScreeningJAMA, 2016
- NGS-Based Assay for the Identification of Individuals Carrying Recessive Genetic Mutations in Reproductive MedicineHuman Mutation, 2016
- Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technologyFertility and Sterility, 2015
- Expanded Carrier Screening in Reproductive Medicine—Points to ConsiderObstetrics & Gynecology, 2015
- Committee Opinion No. 616Obstetrics & Gynecology, 2015
- Ethical and Policy Issues in Genetic Testing and Screening of ChildrenPediatrics, 2013
- ACOG Committee Opinion No. 410: Ethical Issues in Genetic TestingObstetrics & Gynecology, 2008