FAMILIAL ISOLATED PRIMARY HYPERPARATHYROIDISM

被引：3

作者：

WASSIF, WS

PETERS, TJ

机构：

来源：

CLINICAL ENDOCRINOLOGY | 1995年 / 42卷 / 04期

关键词：

D O I：

10.1111/j.1365-2265.1995.tb02656.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：441 / 442

页数：2

共 8 条

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[2] A MINISATELLITE AND A MICROSATELLITE POLYMORPHISM WITHIN 1.5-KB AT THE HUMAN MUSCLE GLYCOGEN-PHOSPHORYLASE (PYGM) LOCUS CAN BE AMPLIFIED BY PCR AND HAVE COMBINED INFORMATIVENESS OF PIC-0.95 [J].

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[3] FAMILIAL ISOLATED PRIMARY HYPERPARATHYROIDISM [J].

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[4] PREDICTIVE TESTING FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 USING DNA POLYMORPHISMS [J].

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[6] STUDIES IN A KINDRED WITH PARATHYROID CARCINOMA [J].

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[7] ASSOCIATION OF PARATHYROID TUMORS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 WITH LOSS OF ALLELES ON CHROMOSOME-11 [J].

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[8] FAMILIAL ISOLATED HYPERPARATHYROIDISM - A DISTINCT GENETIC ENTITY WITH AN INCREASED RISK OF PARATHYROID CANCER [J].

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MONIZ, CF ;

FRIEDMAN, E ;

WONG, S ;

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NORDENSKJOLD, M ;

PETERS, TJ ;

LARSSON, C .

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