Wolf Hirschhorn Syndrome Trust for the UK and Ireland.

Do you need to talk to someone? Welcome to the official site of the Wolf Hirschhorn Syndrome Trust for the UK and Ireland. A national meeting is held once every two years. The group offers advice, support and friendship to anyone with an interest in Wolf Hirschhorn Syndrome and we hope to hear from you soon. Our newsletters are here. Dr John Careys Research. Visit our message board. Have you got a question? Do you have a suggestion? Maybe you could give some advice. Welcome to whs4pminus.co.uk.

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4p- Support Group

Our 2014 National Conference Sponsors. Welcome to the 4P- Support Group. 2014 National Conference GOLD Level Sponsors. 2014 National Conference Gold Level Sponsors. 2014 National Conference SILVER Level Sponsors. Meet our children with Wolf-Hirschhorn and 4p related conditions. 2014 National Conference Harrisburg, PA Brochure and Registration.

Kians Hope - Home

Giving hope to help families of Children and Adults with Wolf Hirschhorn Syndrome. Welcome to our website, we want to raise awareness of Kian, our 3 year old son who suffers with this syndrome, but we also want to raise awareness and project positivity to give hope to families in the same situation. We are Craig and Madeline Henaghan and we are proud parents of Kian, he was born January 2007 at Rake Lane weighing 4lb 15oz. Kian Birth - 3 years.

Asociación Española del Síndrome Wolf-Hirschhorn

Aproximación al SWH y principales características. Comparte tus experiencias con el resto de familias. Mapa de personas con SWH en España. Vídeos de las IV Jornadas Médicas y de Apoyo Familiar del SWH 2015. A continuación os dejamos los vídeos de actividades de las IV Jornadas Médicas y de Apoyo Familiar del SWH 2015. Celebradas el 1 y 2 de mayo de 2015.

Etusivu KV-tietopankki

Käyttäjäkyselyn tuloksia käytetään KV-tietopankin sisällön kehittämiseen. Uusi terveyden edistämisestä kertova osio on avattu! Löydät tietoa unesta sekä suun ja hampaiden terveydestä. Lähiaikoina myös ravitsemuksesta ja liikunnasta.

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Wolf Hirschhorn Syndrome Trust for the UK and Ireland.

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Do you need to talk to someone? Welcome to the official site of the Wolf Hirschhorn Syndrome Trust for the UK and Ireland. A national meeting is held once every two years. The group offers advice, support and friendship to anyone with an interest in Wolf Hirschhorn Syndrome and we hope to hear from you soon. Our newsletters are here. Dr John Careys Research. Visit our message board. Have you got a question? Do you have a suggestion? Maybe you could give some advice. Welcome to whs4pminus.co.uk.

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The website has the following in the web site, "Do you need to talk to someone? Welcome to the official site of the Wolf Hirschhorn Syndrome Trust for the UK and Ireland." I analyzed that the web site also stated " A national meeting is held once every two years." They also stated " The group offers advice, support and friendship to anyone with an interest in Wolf Hirschhorn Syndrome and we hope to hear from you soon. Have you got a question? Do you have a suggestion? Maybe you could give some advice."

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Washburn High School Class of 1961 50th Reunion Home

Washburn High School Class of 1961 50th Reunion. Ramsey JrHS Class of 1958. Ramsey JrHS Class of 1958. Come Join us as we celebrate our 50th Anniversary on September 9-11, 2011. We have a weekend of fun planned - make sure you are here to enjoy the festivities.

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Last update; 27 February 2015. Bring out you stories! Dave Newcomer is seeking stories and remembrances from our years at WHS for inclusion in his talk at the upcoming reunion. He promises complete anonymity for the perpetrators. Send your material to Doctor Dave;. Please send additional material to Al Klase. Picnic in the Park 2014 -. The Reunion Photo Album .