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5. A study on the inheritance of thyroxine-binding globulin (TBG) deficiency from data obtained in 13 families detected by a neonatal screening program. Charbonneau M; Dussault JH; Refetoff S; Takamatsu J; Letarte J; Laberge C Clin Invest Med; 1988 Feb; 11(1):34-9. PubMed ID: 3130208 [TBL] [Abstract][Full Text] [Related]
6. [Familial disorders of thyroxin-binding globulin as a cause of misleading serum thyroxin values. A study of 6 families]. Bürgi H; Zuppinger K; Köchli HP; Burger A Schweiz Med Wochenschr; 1974 Aug; 104(33):1141-7. PubMed ID: 4216956 [No Abstract] [Full Text] [Related]
7. Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene. Narendran P; Lado-Abeal J; Moeller LC; Refetoff S Clin Endocrinol (Oxf); 2003 Dec; 59(6):824-5. PubMed ID: 14974930 [No Abstract] [Full Text] [Related]
8. Inherited thyroxine-binding globulin excess. Study in a kindred. Frank K; Gärtner R; Raue F; Ziegler R Exp Clin Endocrinol; 1986 Dec; 88(2):237-41. PubMed ID: 3104070 [TBL] [Abstract][Full Text] [Related]
9. A novel mutation causing complete thyroxine-binding globulin deficiency (TBG-CD-Negev) among the Bedouins in southern Israel. Miura Y; Hershkovitz E; Inagaki A; Parvari R; Oiso Y; Phillip M J Clin Endocrinol Metab; 2000 Oct; 85(10):3687-9. PubMed ID: 11061524 [TBL] [Abstract][Full Text] [Related]
10. Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping. Reutrakul S; Dumitrescu A; Macchia PE; Moll GW; Vierhapper H; Refetoff S J Clin Endocrinol Metab; 2002 Mar; 87(3):1045-51. PubMed ID: 11889160 [TBL] [Abstract][Full Text] [Related]
12. Metabolism of thyroxine-binding globulin in man. Abnormal rate of synthesis in inherited thyroxine-binding globulin deficiency and excess. Refetoff S; Fang VS; Marshall JS; Robin NI J Clin Invest; 1976 Feb; 57(2):485-95. PubMed ID: 56342 [TBL] [Abstract][Full Text] [Related]
13. Gene amplification as a cause of inherited thyroxine-binding globulin excess in two Japanese families. Mori Y; Miura Y; Takeuchi H; Igarashi Y; Sugiura J; Saito H; Oiso Y J Clin Endocrinol Metab; 1995 Dec; 80(12):3758-62. PubMed ID: 8530630 [TBL] [Abstract][Full Text] [Related]
14. [Inborn defect of thyroxine binding globulin (TBG) diagnosed during screening for congenital hypothyroidism]. Hníková O; Kracmar P Cesk Pediatr; 1983 Jul; 38(7):416-8. PubMed ID: 6413079 [No Abstract] [Full Text] [Related]
15. Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptide. Fingerhut A; Reutrakul S; Knuedeler SD; Moeller LC; Greenlee C; Refetoff S; Janssen OE J Clin Endocrinol Metab; 2004 May; 89(5):2477-83. PubMed ID: 15126580 [TBL] [Abstract][Full Text] [Related]
16. Complete thyroxine-binding globulin (TBG) deficiency produced by a mutation in acceptor splice site causing frameshift and early termination of translation (TBG-Kankakee). Carvalho GA; Weiss RE; Refetoff S J Clin Endocrinol Metab; 1998 Oct; 83(10):3604-8. PubMed ID: 9768672 [TBL] [Abstract][Full Text] [Related]