VARIANT OF IDURONIDASE DEFICIENT MUCOPOLYSACCHARIDOSES - FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY

被引：12

作者：

DANES, BS ^{[1
]}

机构：

[1] CORNELL UNIV,SCH MED,DEPT MED,CELL GENET LAB,NEW YORK,NY 10021

来源：

JOURNAL OF MEDICAL GENETICS | 1977年 / 14卷 / 05期

关键词：

D O I：

10.1136/jmg.14.5.346

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：346 / 351

页数：6

共 17 条

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NEUFELD, EF .

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[4]

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[5]

DANES BS, 1974, LANCET, V1, P680

[6] HURLERS SYNDROME - A GENETIC STUDY OF CLONES IN CELL CULTURE WITH PARTICULAR REFERENCE TO LYON HYPOTHESIS [J].

DANES, BS ;

BEARN, AG .

JOURNAL OF EXPERIMENTAL MEDICINE, 1967, 126 (03) :509-&

[7]

DANES BS, 1976, BIRTH DEFECTS RISKS, P297

[8]

DIFERRANTE N, 1972, CONNECTIVE TISSUE RE, V1, P93

[9] MUCOPOLYSACCHARIDES IN URINE DURING NORMAL HUMAN DEVELOPMENT [J].

DOUGLAS, C ;

NOWAK, J ;

DANES, BS .

PEDIATRIC RESEARCH, 1973, 7 (08) :724-727

[10]

LEISTI J, 1975, LANCET, V1, P1344

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