Few studies have been conducted comparing the FMR1 mutation in multiple tissues of individuals affected with fragile X syndrome. We report a postmortem study of the FMR1 mutation in multiple tissues from a high-functioning male with fragile X syndrome. This man was not mentally retarded and had only
Metaphyseal dysostosis and congenital nystagmus in a male infant with the fragile X syndrome
✍ Scribed by Williams, Charles A. ;Cantú, Eduardo S. ;Frías, Jaime L. ;Opitz, John M. ;Reynolds, James F.
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 266 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0148-7299
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