THE FRAGILE X-SYNDROME - THE PATIENTS AND THEIR CHROMOSOMES

被引:23
作者
DEARCE, MA [1 ]
KEARNS, A [1 ]
机构
[1] ST MICHAELS HOUSE,DUBLIN 14,IRELAND
关键词
D O I
10.1136/jmg.21.2.84
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:84 / 91
页数:8
相关论文
共 83 条
[11]  
DEARCE MA, 1983, CLIN GENET, V24, P320
[12]  
DEROOVER J, 1977, ANN GENET-PARIS, V20, P263
[13]   THE EXPRESSION OF FRAGILE X-CHROMOSOMES IN MEMBERS OF THE SAME FAMILY AT DIFFERENT TIMES OF EXAMINATION [J].
EBERLE, G ;
ZANKL, M ;
ZANKL, H .
HUMAN GENETICS, 1982, 61 (03) :254-255
[14]  
ESCALANTE JA, 1971, J GENET HUM, V19, P137
[15]   THE DIAGNOSIS AND FREQUENCY OF X-LINKED CONDITIONS IN A COHORT OF MODERATELY RETARDED MALES WITH AFFECTED BROTHERS [J].
FISHBURN, J ;
TURNER, G ;
DANIEL, A ;
BROOKWELL, R .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (04) :713-724
[16]  
FITZSIMMONS J, 1982, PRACTITIONER, V226, P735
[17]   A SIMPLE METHOD TO DEMONSTRATE THE FRAGILE X-CHROMOSOME IN FIBROBLASTS [J].
FONATSCH, C .
HUMAN GENETICS, 1981, 59 (02) :186-186
[18]   SCREENING FOR FRA(X)(Q) IN A POPULATION OF MENTALLY-RETARDED MALES [J].
FROSTERISKENIUS, U ;
FELSCH, G ;
SCHIRREN, C ;
SCHWINGER, E .
HUMAN GENETICS, 1983, 63 (02) :153-157
[19]  
FRYNS JP, 1983, CLIN GENET, V23, P203
[20]   TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S) [J].
FRYNS, JP ;
VANDENBERGHE, H .
HUMAN GENETICS, 1982, 61 (03) :262-263