Search Results - Possato, Roberta F.

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  1. 1
    The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

    The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation by Pardo, Viviane, Vono-Toniolo, Jussara, Rubio, Ileana G. S., Knobel, Meyer, Possato, Roberta F., Targovnik, Hector M., Kopp, Peter, Medeiros-Neto, Geraldo

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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

    A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation 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

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