Refining reproductive risk for FMR1 premutation carriers in the general obstetric population
Author:
Affiliation:
1. Progenity, Inc. Ann Arbor Michigan USA
2. Asuragen, Inc. Austin Texas USA
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62666
Reference23 articles.
1. Preconceptional and prenatal screening for fragile X syndrome: Experience with 40 000 tests
2. A Genotype-Phenotype Study of High-Resolution FMR1 Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments
3. An Information-Rich CGG Repeat Primed PCR That Detects the Full Range of Fragile X Expanded Alleles and Minimizes the Need for Southern Blot Analysis
4. Committee Opinion No. 690: Carrier Screening in the Age of Genomic Medicine
5. Committee Opinion No. 691: Carrier Screening for Genetic Conditions
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