RISK FOR CHROMOSOME ABNORMALITY AT AMNIOCENTESIS FOLLOWING A CHILD WITH A NON-INHERITED CHROMOSOME ABERRATION - A EUROPEAN COLLABORATIVE STUDY ON PRENATAL DIAGNOSES 1981

被引:52
作者
STENE, J [1 ]
STENE, E [1 ]
MIKKELSEN, M [1 ]
机构
[1] JF KENNEDY INST,DEPT MED GENET,DK-2600 GLOSTRUP,DENMARK
关键词
D O I
10.1002/pd.1970040707
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
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页码:81 / 95
页数:15
相关论文
共 35 条
[1]  
ALFI OS, 1980, AM J HUM GENET, V32, P477
[2]  
AYME S, 1979, CLIN GENET, V15, P78
[3]  
BERNHEIM A, 1979, ANN GENET-PARIS, V22, P112
[4]  
BOUE A, 1979, PRENATAL DIAGNOSIS, P35
[5]   RISK OF PARENTS WHO HAVE HAD ONE CHILD WITH DOWNS SYNDROME (MONGOLISM) HAVING ANOTHER CHILD SIMILARLY AFFECTED [J].
CARTER, CO ;
EVANS, KA .
LANCET, 1961, 2 (720) :785-&
[6]  
FERGUSONSMITH MA, 1979, PRENATAL DIAGNOSIS, P1
[7]  
FORSSMAN H., 1967, CIBA FOUND STUDY GROUP, V25, P23
[8]   EUROPEAN EXPERIENCE WITH PRENATAL DIAGNOSIS OF CONGENITAL DISEASE - SURVEY OF 6121 CASES [J].
GALJAARD, H .
CYTOGENETICS AND CELL GENETICS, 1976, 16 (06) :453-467
[9]  
HAMERTON J, 1982, HUMAN GENETICS B, P369
[10]  
HAMERTON JL, 1961, LANCET, V2, P788