Weiss RE

References (3)

Title : Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism - Bruellman_2020_J.Clin.Endocrinol.Metab_105_1564
Author(s) : Bruellman RJ , Watanabe Y , Ebrhim RS , Creech MK , Abdullah MA , Dumitrescu AM , Refetoff S , Weiss RE
Ref : J Clinical Endocrinology Metab , 105 :1564 , 2020
Abstract :
PubMedSearch : Bruellman_2020_J.Clin.Endocrinol.Metab_105_1564
PubMedID: 31867598

Title : Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism - Bruellman_2020_Thyroid__
Author(s) : Bruellman R , Watanabe Y , Shareef R , Abdullah MA , Dumitrescu A , Strauss BS , Refetoff S , Weiss RE
Ref : Thyroid , : , 2020
Abstract :
PubMedSearch : Bruellman_2020_Thyroid__
PubMedID: 31868128

Title : A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report - Watanabe_2018_BMC.Med.Genet_19_69
Author(s) : Watanabe Y , Sharwood E , Goodwin B , Creech MK , Hassan HY , Netea MG , Jaeger M , Dumitrescu A , Refetoff S , Huynh T , Weiss RE
Ref : BMC Med Genet , 19 :69 , 2018
Abstract :
PubMedSearch : Watanabe_2018_BMC.Med.Genet_19_69
PubMedID: 29720101
Gene_locus related to this paper: human-TG