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Turner syndrome is a genetic condition, rare, due to the total or partial absence of one X chromosome, affecting 1/2500 newborn female. It combines almost constantly short stature and ovarian failure ...
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Lead Sponsor
University Hospital, Strasbourg, France
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Service de Chirurgie et Médecine Vasculaire, CHU Jean Minjoz
Besançon
Service d'Angiologie, CHU Bocage
Dijon
Service de gynécologie, Centre Médico Chirurgical Obstétrical, Hôpitaux Universitaires
Schiltigheim
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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