GONADAL-DYSGENESIS IN A PATIENT WITH AN X-3 TRANSLOCATION - CASE-REPORT AND REVIEW

被引:23
作者
CARPENTER, NJ
SAY, B
BROWNING, D
机构
[1] UNIV TULSA,CHILDRENS MED CTR,TULSA,OK 74135
[2] UNIV OKLAHOMA,TULSA MED COLL,TULSA,OK
关键词
D O I
10.1136/jmg.17.3.216
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:216 / 221
页数:6
相关论文
共 48 条
[1]  
ALLDERDICE PW, 1971, EXCERPTA MED, V233, P14
[2]   KARYOTYPE-PHENOTYPE CORRELATION IN A 46,XDEL(X) (P22) DIAGNOSIS [J].
BARTSCHSANDHOFF, M ;
TERINDE, R ;
WIEGELMANN, W ;
SCHOLZ, W .
HUMAN GENETICS, 1976, 31 (03) :263-270
[3]   INHERITED X-AUTOSOME TRANSLOCATION IN MAN [J].
BUCKTON, KE ;
JACOBS, PA ;
RAE, LA ;
NEWTON, MS .
ANNALS OF HUMAN GENETICS, 1971, 35 (OCT) :171-&
[4]   PRESUMPTIVE EVIDENCE OF 2 ACTIVE X CHROMOSOMES IN SOMATIC-CELLS OF A HUMAN FEMALE [J].
BUHLER, EM ;
JURIK, LP ;
VOYAME, M ;
BUHLER, UK .
NATURE, 1977, 265 (5590) :142-144
[5]  
CANKI N, 1979, ANN GENET-PARIS, V22, P35
[6]  
COHEN MM, 1972, AM J HUM GENET, V24, P583
[7]  
DAVIS JR, 1976, CLIN GENET, V10, P202
[8]  
DELACHAPELLE A, 1973, CHROMOSOMES TODAY, V4, P261
[9]  
DUTRILLAUX B, 1972, CR ACAD SCI D NAT, V274, P3324
[10]  
Dutrillaux B, 1974, Helv Paediatr Acta, VSuppl 34, P19