| Title : A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation - Rubio_2008_Arq.Bras.Endocrinol.Metabol_52_1337 |
| Author(s) : Rubio IG , Galrao AL , Pardo V , Knobel M , Possato RF , Camargo RR , Ferreira MA , Kanamura CT , Gomes SA , Medeiros-Neto G |
| Ref : Arq Bras Endocrinol Metabol , 52 :1337 , 2008 |
| Abstract : Rubio_2008_Arq.Bras.Endocrinol.Metabol_52_1337 |
| ESTHER : Rubio_2008_Arq.Bras.Endocrinol.Metabol_52_1337 |
| PubMedSearch : Rubio_2008_Arq.Bras.Endocrinol.Metabol_52_1337 |
| PubMedID: 19169491 |
Rubio IG, Galrao AL, Pardo V, Knobel M, Possato RF, Camargo RR, Ferreira MA, Kanamura CT, Gomes SA, Medeiros-Neto G (2008)
A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation
Arq Bras Endocrinol Metabol
52 :1337
Rubio IG, Galrao AL, Pardo V, Knobel M, Possato RF, Camargo RR, Ferreira MA, Kanamura CT, Gomes SA, Medeiros-Neto G (2008)
Arq Bras Endocrinol Metabol
52 :1337