Skip Navigation Home | About CDC | Press Room | Funding | A-Z Index | Centers, Institute & Offices | Training & Employment | Contact Us
CDC Centers for Disease Control and Prevention Home Page
horizontal line  
 

Single Gene Disorders and Disability (SGDD)
Single Gene Disorders Home > Fragile X Syndrome > Resources
Fragile X Syndrome Resources

Conquer Fragile X Foundation (CFXF)
Promotes the development of international fragile X research collaborations to increase the capacity and skills of fragile X labs and researchers around the world, and to encourage young researchers to pursue new and innovative fragile X research projects.

Fragile X Research Foundation (FRAXA)
The Fragile X Research Foundation supports families affected by fragile X and raises awareness of the disease. FRAXA's mission is to find effective treatments and a cure for fragile X by funding research

National Fragile X Foundation (NFXF)
The National Fragile X Foundation is an organization that unites the fragile X community through educational and emotional support and referral networks. NFXF promotes public and professional awareness, and supports research for improved treatments and a cure for fragile X.

National Institute of Child Health and Development – Families and Fragile X Syndrome
The National Institute of Child Health and Human Development (NICHD) is a research agency that is part of the National Institutes of Health. This site provides some general information about fragile X syndrome, its causes, its features, and its treatments.

University of California, Davis - Medical Investigation of Neurodevelopmental Disorders (MIND) Institute – Fragile X Research and Treatment Center
The M.I.N.D. Institute is an international, multidisciplinary research organization focusing on neurodevelopmental disorders. It tries to understand the causes of neurodevelopmental disorders and develop better treatments and hopefully a cure. The Fragile X Research and Treatment Center was established at the M.I.N.D. Institute in 2001.  

AlertProvides link to non-governmental sites and does not necessarily represent the views of the Centers for  Disease Control and Prevention.

 

[Return to top of page]

Date: September 1, 2006
Content source: National Center on Birth Defects and Developmental Disabilities

horizontal line
Topic Contents
 arrow Single Gene Disorders Home
arrow Duchenne/Becker Muscular Dystrophy (DBMD)
arrow Fragile X Syndrome (FXS)
  arrow What is FXS
  arrow Causes
  arrow Inheritance
  arrow Premutation Health
    Problems
  arrow Diagnosis
  arrow CDC Priorities
          arrow CDC Projects
arrow About Genes and Mutations
  arrow X-Linked Conditions
horizontal line
blackdots
Resources
  arrow

 
Duchenne/Becker Muscular Dystrophy (DBMD)
 
  arrow
 
Fragile X Syndrome (FXS)
 
  arrow
 
Genetics at CDC
 
  arrow Other Genetics Resources
     
blackdots
 

Contact Info

Thank you for visiting the CDC-NCBDDD Web site. Click here to contact the National Center on Birth Defects and Developmental Disabilities

For specific medical advice related to these disorders, please contact your health care provider.  For additional questions about the information on this site, please contact cdcinfo@cdc.gov.


 

blackdots
blackdots

National Center on Birth Defects and Developmental Disabilities

National Center on Birth Defects and Developmental Disabilities
 
blackdots

 

    Home   |   Policies and Regulations   |   Disclaimer   |   e-Government   |  FOIA   |  Contact Us  
 Safer, Healthier People  FirstGovDHHS Department of Health
and Human Services
Centers for Disease Control and Prevention,1600 Clifton Rd, Atlanta, GA 30333, U.S.A
Public Inquiries: 1-800-CDC-INFO (232-4636); 1-888-232-6348 (TTY), 24 Hours/Every Day - cdcinfo@cdc.gov