X染色体连锁的家族性甲状腺素结合球蛋白活性降低 - Suppr

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X-chromosome linked familial decrease in thyroxine-binding globulin activity.

作者信息

Nikolai T F, Seal U S

出版信息

J Clin Endocrinol Metab. 1966 Aug;26(8):835-41. doi: 10.1210/jcem-26-8-835.

DOI:10.1210/jcem-26-8-835

PMID:4958593

Abstract

摘要

相似文献

X-chromosome linked familial decrease in thyroxine-binding globulin activity.

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[Hereditary anomalies of globulin transporting thyroxine].

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引用本文的文献

Studies on thyroxine-binding globulin.

J Endocrinol Invest. 1993 May;16(5):353-71. doi: 10.1007/BF03348858.

Familial thyroxine-binding globulin deficiency detected in a pilot screening program for congenital hypothyroidism.

J Endocrinol Invest. 1982 Jan-Feb;5(1):21-5. doi: 10.1007/BF03350477.

Genetic polymorphism of thyroxin-binding globulin (TBG) in the Pacific area.

Am J Hum Genet. 1984 May;36(3):646-54.

Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female.

J Endocrinol Invest. 1980 Oct-Dec;3(4):349-52. doi: 10.1007/BF03349369.

Growth retardation and thyroxine-binding globulin deficiency.

Arch Dis Child. 1971 Feb;46(245):115-7. doi: 10.1136/adc.46.245.115.

Familial thyroxine-binding globulin deficiency.

Br Med J. 1970 Jul 4;3(5713):27-9. doi: 10.1136/bmj.3.5713.27.

Thyroid-binding globulin deficiency in a patient with Beckwith's syndrome.

Calif Med. 1973 Apr;118(4):63-6.

X-chromosome linked inheritance of decreased thyroxine-binding globulin.

Arch Dis Child. 1972 Aug;47(254):635-8. doi: 10.1136/adc.47.254.635.

The genetic polymorphism of the thyroxine-binding globulin (TBG).

Humangenetik. 1972;14(2):85-94. doi: 10.1007/BF00273290.

Familial thyroxine-binding globulin deficiency: search for linkage with Xg blood groups.

J Med Genet. 1974 Sep;11(3):271-4. doi: 10.1136/jmg.11.3.271.

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