PRENATAL-DIAGNOSIS OF MAROTEAUX-LAMY SYNDROME

被引：0

作者：

VANDYKE, DL

FLUHARTY, AL

SCHAFER, IA

SHAPIRO, LJ

KIHARA, H

WEISS, L

机构：

[1] UNIV CALIF LOS ANGELES,PACIFIC STATE HOSP,INST NEUROPSYCHIAT,RES GRP,POMONA,CA

[2] CASE WESTERN RESERVE UNIV,CLEVELAND METROPOLITAN GEN HOSP,DEPT PEDIAT,CLEVELAND,OH 44109

[3] UNIV CALIF LOS ANGELES,HARBOR GEN HOSP,DEPT PEDIAT,TORRANCE,CA 90509

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1981年 / 8卷 / 02期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：235 / 242

页数：8

共 9 条

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SPENCER, B .

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[2] ARYLSULFATASE B DEFICIENCY IN MAROTEAUX-LAMY SYNDROME - CELLULAR STUDIES AND CARRIER IDENTIFICATION [J].

BERATIS, NG ;

TURNER, BM ;

WEISS, R ;

HIRSCHHORN, K .

PEDIATRIC RESEARCH, 1975, 9 (05) :475-480

[3]

CANTZ M, 1972, METHOD ENZYMOL, V28, P884

[4] ARYLSULFATASE-B DEFICIENCY IN MAROTEAUX-LAMY SYNDROME CULTURED FIBROBLASTS [J].

FLUHARTY, AL ;

STEVENS, RL ;

SANDERS, DL ;

KIHARA, H .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1974, 59 (02) :455-461

[5]

FUJIMOTO A, 1978, CLIN CHIM ACTA, V90, P157

[6]

KABACK M M, 1970, New England Journal of Medicine, V282, P1336, DOI 10.1056/NEJM197006112822403

[7]

KLEIJER WJ, 1976, LANCET, V2, P50

[8]

VANBIERVLIET JPGM, 1977, ARCH FR PEDIATR, V34, P362

[9]

VANDYKE DL, 1979, PEDIATR RES, V13, P427

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