Title : Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations - Pardo_2008_Thyroid_18_783 |
Author(s) :
Pardo V , Rubio IG , Knobel M , Aguiar-Oliveira MH , Santos MM , Gomes SA , Oliveira CR , Targovnik HM , Medeiros-Neto G |
Ref :
Thyroid , 18 :783 , 2008 |
Abstract : Pardo_2008_Thyroid_18_783 |
ESTHER : Pardo_2008_Thyroid_18_783 |
PubMedSearch : Pardo_2008_Thyroid_18_783 |
PubMedID: 18631008 |
Gene_locus related to this paper:
human-TG |