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 |