The Fragile X Registry

The Fragile X Registry is for families affected by Fragile X Syndrome. It is a collaboration between NHS Scotland Clinical Genetics services and the Patrick Wild Centre and is currently funded by a grant from the R.S. Macdonald Charitable Trust. The aim of the Registry is to acquire detailed clinical data on individuals who carry either the full mutation or the premutation of the Fragile X gene.

Update: We apologise for the delay in starting the Registry but things are now progressing!  We have recently recruited a clinical psychologist to develop the project and are now hoping to be up and running by the end of 2012.

Please check back to this page for updates.

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