Pardo_2008_Thyroid_18_783

Reference

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

Related information

Gene_locus related to this paper: human-TG

Citations formats

Pardo V, Rubio IG, Knobel M, Aguiar-Oliveira MH, Santos MM, Gomes SA, Oliveira CR, Targovnik HM, Medeiros-Neto G (2008)
Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations
Thyroid 18 :783

Pardo V, Rubio IG, Knobel M, Aguiar-Oliveira MH, Santos MM, Gomes SA, Oliveira CR, Targovnik HM, Medeiros-Neto G (2008)
Thyroid 18 :783