HETEROZYGOTE DETECTION IN HUNTER SYNDROME

被引：16

作者：

ZLOTOGORA, J

BACH, G

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1984年 / 17卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320170317

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：661 / 665

页数：5

共 16 条

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[2] DEFECT IN HUNTER SYNDROME - DEFICIENCY OF SULFOIDURONATE SULFATASE [J].

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[3]

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[4]

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[5] MOSAICISM FOR SULFOIDURONATE SULFATASE DEFICIENCY IN CARRIERS OF HUNTERS SYNDROME [J].

CAPOBIANCHI, MR ;

ROMEO, G .

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[6]

DONNELLY PV, 1975, PEDIATRICS, V56, P429

[7]

EPSTEIN CJ, 1976, LANCET, V2, P737

[8]

Hall C W, 1978, Methods Enzymol, V50, P439

[9] IDURONATE SULFATASE ACTIVITY IN SERUM, LYMPHOCYTES, AND FIBROBLASTS - SIMPLIFIED DIAGNOSIS OF HUNTER SYNDROME [J].

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[10]

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