FAMILIAL THYROXINE-BINDING GLOBULIN DEFICIENCY IN A PATIENT WITH TURNERS SYNDROME (XO) - GENETIC STUDY OF A KINDRED

被引：77

作者：

REFETOFF, S

SELENKOW, HA

机构：

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1968年 / 278卷 / 20期

关键词：

D O I：

10.1056/NEJM196805162782002

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

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页码：1081 / &

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