FLUORESCENCE AND AUTORADIOGRAPHIC STUDIES IN PATIENTS WITH TURNERS SYNDROME AND 46,XXP- AND 46,XXQ- KARYOTYPES

被引:36
作者
BOCZKOWSKI, K
MIKKELSEN, M
机构
[1] MED ACAD WARSAW, INST OBSTET & GYNAECOL, DIV GENET, WARSAW, POLAND
[2] JOHN F KENNEDY INST, GLOSTRUP, DENMARK
关键词
D O I
10.1136/jmg.10.4.350
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:350 / 355
页数:6
相关论文
共 20 条
  • [1] ALLDERDICE PW, 1971, EXCERPTA MEDICA 233, P14
  • [2] PARTIAL DELETION OF AN X CHROMOSOME
    ATKINS, L
    SANTESSON, B
    VOSS, H
    [J]. ANNALS OF HUMAN GENETICS, 1965, 29 : 89 - +
  • [3] SOMATIC STIGMATA OF TURNERS SYNDROME IN A PATIENT WITH 46,XXQ-
    BOCIAN, M
    KRMPOTIC, E
    SZEGO, K
    ROSENTHAL, IM
    [J]. JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) : 358 - +
  • [4] INHERITED X-AUTOSOME TRANSLOCATION IN MAN
    BUCKTON, KE
    JACOBS, PA
    RAE, LA
    NEWTON, MS
    [J]. ANNALS OF HUMAN GENETICS, 1971, 35 (OCT) : 171 - &
  • [5] CASPERSSON T, 1970, CHROMOSOMA, V30, P215
  • [6] DUCOS J, 1971, LANCET, V2, P219
  • [7] FERGUSON-SMITH M A, 1965, J Med Genet, V2, P142, DOI 10.1136/jmg.2.2.142
  • [8] FRACCARO M, 1964, CYTOGENETICS CELLS C, pCH3
  • [9] GIANNELLI F, 1970, HUMAN CHROMOSOMES DN, pCH5
  • [10] HECHT F, 1970, Journal of Medical Genetics, V7, P1, DOI 10.1136/jmg.7.1.1