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 review...
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| Main Authors: | , , , |
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| Format: | Book |
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Mary Ann Liebert,
2021-11-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |