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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Detalles Bibliográficos
Autores principales: Reiss, Sarah, Zalles, Laura, Gbekie, Catherine, Lozano, Reymundo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617583/
https://www.ncbi.nlm.nih.gov/pubmed/34841396
http://dx.doi.org/10.1089/whr.2021.0059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617583/
https://www.ncbi.nlm.nih.gov/pubmed/34841396
http://dx.doi.org/10.1089/whr.2021.0059

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