Turner Syndrome Society Of The United States
Non Profit Organization Management, West Rd, Houston, , 77065, Texas, 11250, United States, 1-10 Employees
Phone Number: +18*********
Who is TURNER SYNDROME SOCIETY OF THE UNITED STATES
The Turner Syndrome Society of the United States advances knowledge, facilitates research, and provides support for all touched by Turner syndrome. Turner syndrome (TS) is a chromosomal c...
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Headquarters: 11250 West Rd, Houston, Texas, 77065, United States
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Date Founded: 1987
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Employees: 1-10
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Revenue: $1 Million to $5 Million
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Active Tech Stack: See technologies
Industry: Non Profit Organization Management
SIC Code: 8399
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NAICS Code: 813990 |
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Frequently Asked Questions Regarding Turner Syndrome Society of the United States
Answer: Turner Syndrome Society of the United States's headquarters are located at West Rd, Houston, , 77065, Texas, 11250, United States
Answer: Turner Syndrome Society of the United States's phone number is +18*********
Answer: Turner Syndrome Society of the United States's official website is https://turnersyndrome.org
Answer: Turner Syndrome Society of the United States's revenue is $1 Million to $5 Million
Answer: Turner Syndrome Society of the United States's SIC: 8399
Answer: Turner Syndrome Society of the United States's NAICS: 813990
Answer: Turner Syndrome Society of the United States has 1-10 employees
Answer: Turner Syndrome Society of the United States is in Non Profit Organization Management
Answer: Turner Syndrome Society of the United States contact info: Phone number: +18********* Website: https://turnersyndrome.org
Answer: The Turner Syndrome Society of the United States advances knowledge, facilitates research, and provides support for all touched by Turner syndrome. Turner syndrome (TS) is a chromosomal condition that describes girls and women with common features that are caused by complete or partial absence of the second sex chromosome. The syndrome is named after Dr. Henry Turner, who was among the first to describe its features in the 1930's. TS occurs in approximately 1 of every 2,000 female births. Diagnosis is made through a test called a karyotype, which is usually performed on cells in the amniotic fluid before birth, and on cells in the blood after birth.
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