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skip to main content about us history of the charity become a member trustees newsletters events contact us noonan syndrome the syndrome family stories publications our work supporting families funding research raising awareness families days our experts medical advisory group support us make a donation fundraise leave a legacy menu about us history of the charity become a member trustees newsletters events contact us noonan syndrome the syndrome family stories publications our work supporting families funding research raising awareness families days our experts medical advisory group support us make a donation fundraise leave a legacy £10,560 / £15,000 to fund our next research project we need £15,000 – we are getting there but we need your help! we support families through a dedicated medical advisory group, events and publications. we fund medical research to advance improvements in the understanding, care and management of the condition. we improve awareness of the condition and its impact on the lives of those affected. recent news 2019 families day and activities weekend – date announced! april 30, 2018 following on from the success of this year’s families day and activities weekend, we are happy to be able to confirm that next year’s event will be held over the … read more » families for families day – 21st april april 9, 2018 our families for families day approaches with less than a fortnight to go. here’s the latest version of our programme for saturday. we can still accept families wanting to attend … read more » families for families day april 21st 2018 february 13, 2018 our next families for families day is on saturday 21st april at the whitemoor lakes centre near lichfield in staffordshire and this year you can also make a weekend of … read more » noonan syndrome awareness month february 6, 2018 our friends in the usa – the noonan syndrome foundation – have made february noonan syndrome awareness month. let’s do our bit: read more » a merry christmas and a happy and peaceful new year from noonan syndrome association december 24, 2017 read more » families for families day & activities weekend 20th to 22nd april 2018 november 28, 2017 as usual our families for families day will be taking place in spring, on saturday 21st april 2018 and we’ll have more details in the new year about registering to … read more » 2018 families day and activities weekend september 22, 2017 the 2018 families day will be on saturday 21st april. and next year, it will be happening alongside – and as part of – a members’ activities weekend, with everything … read more » the nsa is dedicated to supporting people and families affected by noonan syndrome and related conditions (on the ras/mapk pathway) in the uk to continue with our work we urgently need your support. donate now online, send a donation or leave a legacy in your will. join the 'reach out campaign' to support the nsa through a regular giving scheme. fundraise through events, sponsorships & challenges at work or with friends. registered charity no. 1140671 support for individuals and families affected by noonan syndrome in the uk medical adviser: professor michael a patton frcp correspondence address: 12 talbot close, shifnal, shropshire tf11 8sg principal address: cross chambers, 9 high street, newtown, powys, sy16 2ny © 2018 noonan syndrome association developed by vr solutions by using this site you agree to our cookie & privacy policy. accept read more privacy policy

URL analysis for noonansyndrome.org.uk

http://www.noonansyndrome.org.uk/families-for-families-day-april-21st-2018/
http://www.noonansyndrome.org.uk/families-days/
http://www.noonansyndrome.org.uk/families-for-families-day-activities-weekend-20th-to-22nd-april-2018/
http://www.noonansyndrome.org.uk/app/download/5803729235/standing-order-form.pdf
http://www.noonansyndrome.org.uk/medical-advisory-board/
http://www.noonansyndrome.org.uk/privacy-policy/
http://www.noonansyndrome.org.uk/trustees/
http://www.noonansyndrome.org.uk/leave-a-legacy/
http://www.noonansyndrome.org.uk/
http://www.noonansyndrome.org.uk/2018-families-day-and-activities-weekend/
http://www.noonansyndrome.org.uk/contact-us/
http://www.noonansyndrome.org.uk/fundraise/
http://www.noonansyndrome.org.uk/raising-awareness/
http://www.noonansyndrome.org.uk/newsletters/
http://www.noonansyndrome.org.uk/funding-research/

Whois Information

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Error for "noonansyndrome.org.uk".

the WHOIS query quota for 2600:3c03:0000:0000:f03c:91ff:feae:779d has been exceeded
and will be replenished in 136 seconds

WHOIS lookup made at 15:35:11 15-Jul-2017

--
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for .uk domain names. This information and the .uk WHOIS are:

Copyright Nominet UK 1996 - 2017.

You may not access the .uk WHOIS or use any data from it except as permitted
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  REFERRER http://www.nominet.org.uk

  REGISTRAR Nominet UK

SERVERS

  SERVER uk.whois-servers.net

  ARGS noonansyndrome.org.uk

  PORT 43

  TYPE domain

DISCLAIMER
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:
Copyright Nominet UK 1996 - 2017.
You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REGISTERED no

DOMAIN

  NAME noonansyndrome.org.uk

NSERVER

  NS67.1AND1.CO.UK 217.160.80.173

  NS68.1AND1.CO.UK 217.160.81.173

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