FAMILIAL THYROXINE-BINDING GLOBULIN DEFICIENCY

被引：23

作者：

TORKINGT.P

HARRISON, RJ

MACLAGAN, NF

BURSTON, D

机构：

来源：

BRITISH MEDICAL JOURNAL | 1970年 / 3卷 / 5713期

关键词：

D O I：

10.1136/bmj.3.5713.27

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：27 / &

共 11 条

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[3]

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[6] X-CHROMOSOME LINKED INHERITANCE OF THYROXINE-BINDING GLOBULIN DEFICIENCY [J].

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[7] THYROXINE BINDING GLOBULIN (TBG) DEFICIENCY - A PROBLEM IN DIAGNOSIS OF THYROID DISEASE [J].

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[8] X-CHROMOSOME LINKED FAMILIAL DECREASE IN THYROXINE-BINDING GLOBULIN ACTIVITY [J].

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[9] FAMILIAL THYROXINE-BINDING GLOBULIN DEFICIENCY IN A PATIENT WITH TURNERS SYNDROME (XO) - GENETIC STUDY OF A KINDRED [J].

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[10] EUTHYROID MAN WITHOUT THYROXINE-BINDING GLOBULIN [J].

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STARR, P .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1959, 19 (04) :485-487

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