Turner Syndrome Foundation
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- The Turner Syndrome Foundation is dedicated in its mission to advance communications about Turner Syndrome, a chromosomal abnormality that affects 1 in 2,000 females. It has a board of directors and a well-regarded medical advisory board and a large volunteer base that assists with its advocacy and awareness efforts. The organization strives to create positive outcomes in the lives of girls and women with Turner Syndrome and advocates for legislation that will improve their lives, attends both state and national health conferences, and is involved in continuing medical education grand rounds activities at state hospitals.
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Headquarters:Po Box 726 , Holmdel, New Jersey, United States
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Phone Number: +1 800-594-4585
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Website: https://www.tsfusa.org
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Employees:14
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Revenue:$1 - 10M
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Legal Name:Turner Syndrome Foundation
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Turner Syndrome Foundation's Social Media
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| NAICS Code: 561599 |
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Frequently Asked Questions regarding Turner Syndrome Foundation
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Where are Turner Syndrome Foundation's Headquarters?
Turner Syndrome Foundation's Headquarters are in Po Box 726 ,Holmdel,New Jersey,United States
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What is Turner Syndrome Foundation's phone number?
Turner Syndrome Foundation's phone number is +1 800-594-4585
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What is Turner Syndrome Foundation's official website?
Turner Syndrome Foundation's official website is https://www.tsfusa.org
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What is Turner Syndrome Foundation's Revenue?
Turner Syndrome Foundation's revenue is $1 - 10M
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What is Turner Syndrome Foundation's NAICS code?
Turner Syndrome Foundation's NAICS code is 561599
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How many employees are working in Turner Syndrome Foundation
Turner Syndrome Foundation has 14 employees
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What is Turner Syndrome Foundation's Industry?
Turner Syndrome Foundation is in the industry of Non-Profit Organization Management
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Who is Turner Syndrome Foundation's President?
Turner Syndrome Foundation's President is Laura Fasciano