Fragile X Syndrome: Experiences and Importance of Diagnosis
In this video four parents of individuals with Fragile X are interviewed about their experiences of receiving a diagnosis of Fragile X Syndrome. Professor Andrew Stanfield (Patrick Wild Centre) and Dr Margaretha Van Mourik (Clinical Geneticist) provide expert input. This video was funded by Awards for All, Big Lottery Scotland, as part of the project "Educate to Empower". Through this project the Fragile X Society and the Patrick Wild Centre trained professionals across Scotland about Fragile X Syndrome and produced a resource pack for newly diagnosed families.
▶︎
Fragile Not Broken - Fragile X Documentary
▶︎
Living with Fragile X Syndrome: 'He is maturing ... it's just really slow' | USA TODAY
▶︎
Adult Issues in Fragile X Syndrome
▶︎
A Kid with a Gene Mutation (Fragile X)
▶︎
My Life With Klinefelter's | Journey to Diagnosis
▶︎
Behind the Mystery Fragile X Syndrome: Genetic Disorder That Can Cause Learning/Behavior Challenges
▶︎
Colin Farrell Opens Up About His Son With Angelman Syndrome | PEOPLE
▶︎
Genetics & Diagnosis of Fragile X Syndrome
▶︎
Living with Fragile X
▶︎
Rapid Review (17/175): Fragile X syndrome
▶︎
Fragile X Syndrome: Adulthood & Looking to the Future
▶︎
Fragile X syndrome | Genetics, cell biology and pathology of Fragile X syndrome | USMLE Step 1
▶︎
Living with 12 Alters for 60 Years (A Rare Dissociative Disorder)
▶︎
Fragile X Syndrome: The Stories and the Science
▶︎
The families dealing with Batten Disease | SBS The Feed
▶︎
Living w/ Fragile X | Studio 10
▶︎
Introduction to Fragile X Syndrome
▶︎
Educating Young Children with Fragile X Syndrome
▶︎
The Cognitive Profile of Fragile X syndrome (Dr Marcia Braden)
▶︎