EARLY PRENATAL DIAGNOSIS OF HURLERS SYNDROME WITH TERMINATION OF PREGNANCY AND CONFIRMATORY FINDINGS ON FETUS

被引：32
作者：
CRAWFURD, MD
DEAN, MF
HUNT, DM
JOHNSON, DR
MACDONALD, RR
MUIR, H
PAYLINGW.EA
PAYLINGW.CR
机构：
[1] UNIV LEEDS, DEPT GENET, LEEDS, ENGLAND
[2] UCL, DEPT ANIM GENET, LONDON, ENGLAND
[3] UCL, DEPT HUMAN GENET, LONDON, ENGLAND
[4] KENNEDY INST RHEUMATOL, LONDON, ENGLAND
[5] UNIV LEEDS, DEPT OBSTET & GYNAECOL, LEEDS, ENGLAND
来源：
JOURNAL OF MEDICAL GENETICS | 1973年 / 10卷 / 02期
关键词：
D O I：
10.1136/jmg.10.2.144
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：144 / 153
页数：10
相关论文
共 24 条
[11]   BETA-GALACTOSIDASE DEFICIENCY IN HURLER SYNDROME [J].
MACBRINN, M ;
OKADA, S ;
WOOLLACOTT ;
PATEL, V ;
HO, MW ;
TAPPEL, AL ;
OBRIEN, JS .
NEW ENGLAND JOURNAL OF MEDICINE, 1969, 281 (07) :338-&
[12]  
MATALON R, 1970, LANCET, V1, P83
[13]  
MATALON R, 1972, LANCET, V1, P798
[14]   HURLERS SYNDROME, AN ALPHA-L-IDURONIDASE DEFICIENCY [J].
MATALON, R ;
DORFMAN, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1972, 47 (04) :959-&
[15]  
MCKUSICK VA, 1972, LANCET, V1, P993
[16]   PRENATAL GENETIC DIAGNOSIS .3. [J].
MILUNSKY, A ;
LITTLEFIELD, JW ;
KANFER, JN ;
KOLODNY, EH ;
SHIH, VE ;
ATKINS, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (27) :1498-+
[17]   PRENATAL GENETIC DIAGNOSIS .1. [J].
MILUNSKY, A ;
LITTLEFIELD, JW ;
KANFER, JN ;
KOLODNY, EH ;
SHIH, VE ;
ATKINS, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (25) :1370-+
[18]   PRENATAL GENETIC DIAGNOSIS .2. [J].
MILUNSKY, A ;
LITTLEFIELD, JW ;
KANFER, JN ;
KOLODNY, EH ;
SHIH, VE ;
ATKINS, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (26) :1441-+
[19]   INBORN ERRORS OF MUCOPOLYSACCHARIDE METABOLISM [J].
NEUFELD, EF ;
FRATANTONI, JC .
SCIENCE, 1970, 169 (3941) :141-+
[20]   FRACTIONATION OF 4-METHYLUMBELLIFERYL-BETA-GALACTOSIDASE ACTIVITIES IN LIVER IN GARGOYLISM [J].
OCKERMAN, PA ;
HULTBERG, B .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1968, 22 (03) :199-&
123