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Disorders of growth, puberty and sex development can have genetic causes. The exome analysis could detect new mutations responsible for these disorders and the frequency of these mutations in these di...
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Lead Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
NCT06662045 · Iron-Deficiency Anemia, Neurobehavioral Manifestations, and more
NCT04463316 · Prader-Willi Syndrome, PWS-like Syndrome, and more
NCT03102554 · Disorders of Sex Development, Hypospadias
NCT05382637 · Growth Disorders
NCT04075149 · Polycystic Ovary Syndrome, Puberty Disorders, and more
Hôpital Fondation A de Rothschild
Paris
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Data Source & Attribution
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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