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5. Linkage of thyroxine-binding globulin deficiency to other X-chromosome loci. Bode HH; Rothman KJ; Danon M J Clin Endocrinol Metab; 1973 Jul; 37(1):25-9. PubMed ID: 4197606 [No Abstract] [Full Text] [Related]
6. A TBG-deficient family with a male exhibiting decreased but not zero TBG levels. Roberts RC; Nikolai TF; Lohrenz FN J Clin Endocrinol Metab; 1970 Jan; 30(1):131-3. PubMed ID: 4982597 [No Abstract] [Full Text] [Related]
7. X-chromosome linked inheritance of elevated thyroxine-binding globulin in association with goiter. Shane SR; Seal US; Jones JE J Clin Endocrinol Metab; 1971 May; 32(5):587-94. PubMed ID: 4996058 [No Abstract] [Full Text] [Related]
8. X-chromosome linked inheritance of elevated thyroxine-binding globulin. Jones JE; Seal US J Clin Endocrinol Metab; 1967 Nov; 27(11):1521-8. PubMed ID: 4169433 [No Abstract] [Full Text] [Related]
10. Familial thyroxine-binding globulin deficiency. A study of three Danish families. Strunge P Acta Med Scand; 1974; 195(1-2):5-9. PubMed ID: 4206122 [No Abstract] [Full Text] [Related]
11. X-chromosome linked inheritance of thyroxine-binding globulin deficiency. Nikolai TF; Seal US J Clin Endocrinol Metab; 1967 Nov; 27(11):1515-20. PubMed ID: 4965464 [No Abstract] [Full Text] [Related]
12. Idiopathic or genetic elevation of corticosteroid-binding globulin? Lohrenz F; Doe RP; Seal US J Clin Endocrinol Metab; 1968 Jul; 28(7):1073-5. PubMed ID: 4969809 [No Abstract] [Full Text] [Related]
14. Familial thyroxine-binding globulin deficiency in a patient with Turner's syndrome (XO). Genetic study of a kindred. Refetoff S; Selenkow HA N Engl J Med; 1968 May; 278(20):1081-7. PubMed ID: 4171474 [No Abstract] [Full Text] [Related]
15. [Familial deficiency of thyroxine-binding globulin]. Locher JT; Ruch MH; Marti HR Schweiz Med Wochenschr; 1985 Aug; 115(35):1200-5. PubMed ID: 3931215 [TBL] [Abstract][Full Text] [Related]