Home - National Fragile X Foundation

The parents, scientists, clinicians and staff associated with the National Fragile X Foundation have been committed since the organization was formed in 1984 to help families, spread awareness, find improved treatments, and support research leading to an eventual cure for Fragile X. Please use this website to learn more about Fragile X, and to consider joining our ongoing efforts on behalf of the Fragile X community.

OVERVIEW

The domain fragilex.org presently has an average traffic classification of zero (the lower the higher page views). We have inspected nineteen pages within the web site fragilex.org and found eight hundred and thirty-four websites linking to fragilex.org. There are two contacts and directions for fragilex.org to help you communicate with them. There are four mass communication platforms retained by this website. The domain fragilex.org has been online for one thousand three hundred and twenty-six weeks, ten hours, thirty-two minutes, and eighteen seconds.
Pages Crawled
19
Links to this site
834
Contacts
2
Addresses
2
Social Links
4
Online Since
Feb 1999

FRAGILEX.ORG TRAFFIC

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FRAGILEX.ORG HISTORY

The domain fragilex.org was first documented on February 03, 1999. As of today, it is one thousand three hundred and twenty-six weeks, ten hours, thirty-two minutes, and eighteen seconds young.
REGISTERED
February
1999

PERIOD

25
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CONTACTS

National Fragile X Foundation

National Fragile X Foundation

1615 Bonanza St

Walnut Creek, CA, 94596

US

National Fragile X Foundation

Robby Miller

1615 Bonanza St

Walnut Creek, CA, 94596

US

FRAGILEX.ORG SERVER

We revealed that a single root page on fragilex.org took one thousand eight hundred and twenty-eight milliseconds to load. Our parsers found a SSL certificate, so therefore our parsers consider this site secure.
Load time
1.828 secs
SSL
SECURE
Internet Protocol
50.28.1.219

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SERVER OS

We observed that fragilex.org is using the Apache/2.4.25 (Unix) OpenSSL/1.0.1e-fips mod_bwlimited/1.4 mod_fcgid/2.3.9 os.

HTML TITLE

Home - National Fragile X Foundation

DESCRIPTION

The parents, scientists, clinicians and staff associated with the National Fragile X Foundation have been committed since the organization was formed in 1984 to help families, spread awareness, find improved treatments, and support research leading to an eventual cure for Fragile X. Please use this website to learn more about Fragile X, and to consider joining our ongoing efforts on behalf of the Fragile X community.

PARSED CONTENT

The domain has the following in the web site, "Autism Spectrum Disorder and Fragile X Syndrome." We observed that the web site also stated " Consensus Documents on Clinical Practices." It also stated " News, Reports and Commentaries. National Fragile X Foundation Advocacy Day. National Fragile X Awareness Month. International Parent Support and Clinics. Resources and tools for families."

SEEK OTHER BUSINESSES

Fragile X Association of Australia

Clinics for Children and Adults. What causes Fragile X Syndrome. Are these tests covered by Medicare? What are CGG repeats. What does it mean to be a carrier.

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Fragile X Awareness Fragile X AwarenessFragile X Awareness Spreading Awareness of Fragile X Syndrome and Associated Conditions

Spreading Awareness of Fragile X Syndrome and Associated Conditions. Our site aims to spread awareness of Fragile X Syndrome and the related carrier conditions, FXTAS and FXPOI. We offer information on where to find out more plus what support options are available worldwide.

FRAGILE X B.C.

Welcome to our web site! This site is dedicated to family and friends of people with Fragile X Syndrome in British Columbia. THERE HAVE BEEN ANGELS IN MY LIFE. We invite you to visit us or attend an event. We have several professionals who would be willing to speak with you or answer your questions. Please sign our guestbook to offer comments and join our mailing list.

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