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A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation. [electronic resource] by
- Rubio, Ileana G S
- Galrao, Ana Luiza
- Pardo, Viviane
- Knobel, Meyer
- Possato, Roberta F
- Camargo, Rosalinda R Y
- Ferreira, Marcelo A
- Kanamura, Cristina T
- Gomes, Simone A
- Medeiros-Neto, Geraldo
Producer: 20091007
In:
Arquivos brasileiros de endocrinologia e metabologia vol. 52
Availability: No items available.
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