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Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia
Neonatal screening in Macedonia detects congenital hypothyroidism (CH) with an incidence of 1 in 1,585, and more than 50% of cases exhibit a normally located gland-in-situ (GIS). Monogenic mutations causing dyshormonogenesis may underlie GIS CH; additionally, a small proportion of thyroid hypoplasia...
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| Publicado no: | Front Endocrinol (Lausanne) |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7381236/ https://ncbi.nlm.nih.gov/pubmed/32765423 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.00413 |
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