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2017 Turner Syndrome Conference interview 3. 

Turner Syndrome Society of the United States
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2017 Turner Syndrome Conference interviews with participants.
The Turner Syndrome Society was created in 1987 by a group of women in Minnesota for the purpose of networking and support. Today, we have over 600 members and over 100 volunteers to support and maintain our valuable programs.
We are recognized as national non-profit 501 (c) (3) EIN# 41-1596910 organization providing health-related resources to patients, families, and physicians for the diagnosis and treatment of Turner syndrome. There are chapters and resource groups located throughout the country. The TSSUS is operated by 3 staff members at our National Office in Houston, TX, 2 consultants, and is overseen by 11 nationwide board members.
www.turnersyndrome.org/

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30 авг 2017

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Комментарии : 1   
@wamuyuloise4033
@wamuyuloise4033 Месяц назад
I have a 13 yr old girl diagnosed with classic ts..I would really love her to be part of this conference..but I'm from Kenya..Africa to be precise 😢😢😅..I would really love to know the cost of the conference and an invitation letter for visa processing...is the conference open to us living far off
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