Role of Next Generation Sequencing in the Etiological Diagnosis of Permanent Congenital Hypothyroidism With in Situ Thyroid
Role of Next Generation Sequencing in the Etiological Diagnosis of Permanent Congenital Hypothyroidism With in Situ Thyroid
Recruiting · NCT06728735 · Registry updated 2026-03-12Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Role of Next Generation Sequencing in the Etiological Diagnosis of Permanent Congenital Hypothyroidism With in Situ Thyroid | Bone Diseases, Developmental, Bone Diseases, Endocrine, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dwarfism, bone disorder, congenital hypothyroidism, endocrine system disorder, hereditary disease, hypothyroidism, musculoskeletal system disorder, thyroid gland disorder | Recruiting | Not stated | 2026-03-12 | NCT06728735 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | 331 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Italy | 82 |