PRENATAL DIAGNOSIS OF MAROTEAUX-LAMY SYNDROME

被引:0
作者
KLEIJER, WJ [1 ]
WOLFFERS, GM [1 ]
HOOGEVEEN, A [1 ]
NIERMEIJER, MF [1 ]
机构
[1] ERASMUS UNIV,DEPT CELL BIOL & GENET,ROTTERDAM,NETHERLANDS
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D O I
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中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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页码:50 / 50
页数:1
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[1]   DISTINCT BIOCHEMICAL DEFICIT IN MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS VI) [J].
BARTON, RW ;
NEUFELD, EF .
JOURNAL OF PEDIATRICS, 1972, 80 (01) :114-+
[2]   THE ASSAY OF ARYLSULPHATASE-A AND ARYLSULPHATASE-B IN HUMAN URINE [J].
BAUM, H ;
DODGSON, KS ;
SPENCER, B .
CLINICA CHIMICA ACTA, 1959, 4 (03) :453-455
[3]   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
[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]   DEFECT IN HURLER AND HUNTER SYNDROMES, .2. DEFICIENCY OF SPECIFIC FACTORS INVOLVED IN MUCOPOLYSACCHARIDE DEGRADATION [J].
FRATANTO.JC ;
HALL, CW ;
NEUFELD, EF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1969, 64 (01) :360-&
[6]   METHODOLOGY OF QUANTITATIVE CYTOCHEMICAL ANALYSIS OF SINGLE OR SMALL NUMBERS OF CULTURED-CELLS [J].
GALJAARD, H ;
VANHOOGS.JJ ;
DEJOSSEL.JE ;
MULDER, MP .
HISTOCHEMICAL JOURNAL, 1974, 6 (04) :409-429
[7]   PRENATAL DIAGNOSIS OF TYPE-II GLYCOGENOSIS (POMPES DISEASE) USING MICROCHEMICAL ANALYSES [J].
NIERMEIJER, MF ;
KOSTER, JF ;
JAHODOVA, M ;
FERNANDES, J ;
HEUKELSDULLY, MJ ;
GALJAARD, H .
PEDIATRIC RESEARCH, 1975, 9 (05) :498-503
[8]   MUCOPOLYSACCHARIDOSIS TYPE-VI - (MAROTEAUX-LAMY SYNDROME) .1. SULFATASE-B DEFICIENCY IN TISSUES [J].
STUMPF, DA ;
AUSTIN, JH ;
CROCKER, AC ;
LAFRANCE, M .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1973, 126 (06) :747-755