Centre de référence anomalies du développement de Lyon, Hôpital Femme Mère Enfant
Centre de référence anomalies du développement de Lyon, Hôpital Femme Mère Enfant
Bron, France1 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Study of the Pathophysiology of RNU4ATAC and RTTN Associated Syndromes | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lowry-Wood syndrome, Roifman syndrome, hereditary disease, microcephalic osteodysplastic primordial dwarfism type I, microcephalic osteodysplastic primordial dwarfism types I and III | Recruiting | Not applicable | 2024-10-09 | NCT06111950 |