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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