Identity and Reproductive Aspects in Females with Fragile X Syndrome
Purpose: Fragile X Syndrome (FXS) is caused by a full mutation in the FMR1 gene, defined by >200 CGG repeats. It is the leading cause of inherited intellectual disability, but presents with a wide range of clinical variability in males and particularly amongst females. This article aims to re...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Mary Ann Liebert
2021-11-01
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| Series: | Women's Health Reports |
| Subjects: | |
| Online Access: | https://www.liebertpub.com/doi/full/10.1089/WHR.2021.0059 |