Fragile X syndrome carrier screening accompanied by genetic consultation has clinical utility in populations beyond those recommended by guidelines
Author:
Affiliation:
1. Myriad Women’s Health South San Francisco CA USA
2. Myriad Genetics, Inc. Salt Lake City UT USA
Publisher
Wiley
Subject
Genetics(clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1024
Reference38 articles.
1. Fragile X screening: Attitudes of genetic health professionals
2. Aetna. (2019).Genetic Testing Policy Number 0140. Available athttp://www.aetna.com/cpb/medical/data/100_199/0140.html
3. Committee Opinion No. 469: Carrier Screening for Fragile X Syndrome
4. Committee Opinion No. 691: Carrier Screening for Genetic Conditions
5. Committee Opinion No. 690: Carrier Screening in the Age of Genomic Medicine
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