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Clinical Trial Summary

The protein polymorphism of the growth hormone receptor characterized by the genomic deletion of exon 3 has been linked to the magnitude of the first-year-growth response to growth hormone (GH) in girls with Turner syndrome.

Objective: to study the long-term effect of GH therapy in Turner syndrome in correlation to this GHR polymorphism in a mainly retrospective design (chart-review).


Clinical Trial Description

n/a


Study Design

N/A


Related Conditions & MeSH terms


NCT number NCT00443144
Study type Observational
Source University Hospital Tuebingen
Contact
Status Completed
Phase N/A
Start date May 2005
Completion date May 2007

See also
  Status Clinical Trial Phase
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