PRENATAL DIAGNOSIS OF GENETIC DISEASE

被引:22
作者
HSU, LYF [1 ]
HIRSCHHORN, K [1 ]
机构
[1] MT SINAI SCH MED, DEPT PEDIAT, DIV MED GENET, 100TH ST & FIFTH AVE, NEW YORK, NY 10029 USA
关键词
D O I
10.1016/0024-3205(74)90129-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
引用
收藏
页码:2311 / 2336
页数:26
相关论文
共 66 条
[1]  
AGUERO O, 1970, SURG GYNECOL OBSTETR, V130, P649
[2]  
ALLAN LD, 1973, LANCET, V2, P522
[3]  
[Anonymous], PRENATAL DIAGNOSIS H
[4]  
AULA P, 1973, CLIN GENET, V4, P297
[5]  
BARR ML, 1969, CAN MED ASSOC J, V101, P247
[6]  
BEUTLER E, 1971, AM J HUM GENET, V23, P62
[7]   INHERITED DEFECT AFFECTING TRICARBOXYLIC ACID CYCLE IN A PATIENT WITH CONGENITAL LACTIC ACIDOSIS [J].
BLASS, JP ;
SCHULMAN, JD ;
YOUNG, DS ;
HOM, E .
JOURNAL OF CLINICAL INVESTIGATION, 1972, 51 (07) :1845-&
[8]   QUINACRINE FLUORESCENCE OF HUMAN Y CHROMOSOME [J].
BORGAONKAR, DS ;
HOLLANDER, DH .
NATURE, 1971, 230 (5288) :52-+
[9]  
BROCK DJH, 1972, LANCET, V2, P197
[10]  
BROCK DJH, 1973, LANCET, V2, P923