USE OF QUANTITATIVE CYTOCHEMICAL ANALYSES IN RAPID PRENATAL DETECTION AND SOMATIC-CELL GENETIC STUDIES OF METABOLIC DISEASES

被引:50
作者
GALJAARD, H [1 ]
HOOGEVEEN, A [1 ]
KEIJZER, W [1 ]
DEWITVER.E [1 ]
VLEKNOOT, C [1 ]
机构
[1] ERASMUS UNIV, MED FAC, DEPT CELL BIOL & GENET, ROTTERDAM, NETHERLANDS
来源
HISTOCHEMICAL JOURNAL | 1974年 / 6卷 / 05期
关键词
D O I
10.1007/BF01003266
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
收藏
页码:491 / 509
页数:19
相关论文
共 48 条
[1]   DEFECT IN HURLER AND SCHEIE SYNDROMES - DEFICIENCY OF ALPHA-IDURONIDASE [J].
BACH, G ;
WEISSMAN.B ;
FRIEDMAN, R ;
NEUFELD, EF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) :2048-&
[2]   A MODIFIED URONIC ACID CARBAZOLE REACTION [J].
BITTER, T ;
MUIR, HM .
ANALYTICAL BIOCHEMISTRY, 1962, 4 (04) :330-&
[3]  
BOOTSMA D, 1973, GENETICS, V73, P167
[4]  
BOOTSMA D, 1973, NOBEL S CHROM IDENT
[5]  
BRADY RO, 1972, LIPIDOSIS BIOCHIMIE, V54, P723
[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]   DEMONSTRATION OF 2 POPULATIONS OF CELLS IN HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATEDEHYDROGENASE VARIANTS [J].
DAVIDSON, RG ;
NITOWSKY, HM ;
CHILDS, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1963, 50 (03) :481-&
[8]   CORRECTION OF ENZYMIC DEFECT IN CULTURED FIBROBLASTS FROM PATIENTS WITH FABRYS-DISEASE - TREATMENT WITH PURIFIED ALPHA-GALACTOSIDASE FROM FICIN [J].
DAWSON, G ;
MATALON, R ;
LI, YT .
PEDIATRIC RESEARCH, 1973, 7 (08) :684-690
[9]   MAMMALIAN OOCYTES - X CHROMOSOME ACTIVITY [J].
EPSTEIN, CJ .
SCIENCE, 1969, 163 (3871) :1078-&