Nalaganje...
Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis
OBJECTIVE: Congenital hypothyroidism (CH) is a frequent neonatal endocrine disease with an incidence of about 1:2500 worldwide. Although thyroid dysgenesis (TD) is the most frequent cause of CH cases, its pathogenesis remains unclear. The aim of this study was to screen the hematopoietically-express...
Shranjeno v:
| izdano v: | J Clin Res Pediatr Endocrinol |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Galenos Publishing
2016
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805044/ https://ncbi.nlm.nih.gov/pubmed/26757609 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.2456 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|