EXPERIENCE WITH MULTIPLE APPROACHES TO THE PRENATAL-DIAGNOSIS OF THE FRAGILE-X SYNDROME - AMNIOTIC-FLUID, CHORIONIC VILLI, FETAL BLOOD AND MOLECULAR METHODS

被引:19
作者
SHAPIRO, LR
WILMOT, PL
MURPHY, PD
BREG, WR
机构
[1] NEW YORK MED COLL,DEPT PEDIAT,VALHALLA,NY 10595
[2] NEW YORK MED COLL,DEPT PATHOL,VALHALLA,NY 10595
[3] LETCHWORTH DEV SERV,GENET LAB,THIELLS,NY
[4] YALE UNIV,SCH MED,DEPT HUMAN GENET,NEW HAVEN,CT 06510
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 30卷 / 1-2期
关键词
D O I
10.1002/ajmg.1320300135
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:347 / 354
页数:8
相关论文
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SHAPIRO, LR ;
WILMOT, PL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2) :325-340
[6]  
SHAPIRO LR, 1982, LANCET, V1, P99
[7]  
WEBB T, 1981, LANCET, V2, P1423
[8]  
1985, CYTOGENET CELL GENET, V40, P1