MORPHOLOGY ALONE DOES NOT MAKE AN ISOCHROMOSOME

被引:7
作者
SCHMUTZ, SM [1 ]
PINNO, E [1 ]
机构
[1] REGINA GEN HOSP,CYTOGENET LAB,REGINA,SASKATCHEWAN,CANADA
关键词
D O I
10.1007/BF00291889
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:253 / 255
页数:3
相关论文
共 21 条
  • [1] Misdivision and the genetics of the centromere
    Darlington, CD
    [J]. JOURNAL OF GENETICS, 1939, 37 (02) : 341 - U19
  • [2] The origin of iso-chromosomes
    Darlington, CD
    [J]. JOURNAL OF GENETICS, 1940, 39 (02) : 351 - 361
  • [3] HOW DO HUMAN ISOCHROMOSOMES ARISE
    DELACHAPELLE, A
    [J]. CANCER GENETICS AND CYTOGENETICS, 1982, 5 (02) : 173 - 179
  • [4] FROSTERISKENIUS U, 1984, CLIN GENET, V26, P549
  • [5] TRISOMY-9P WITH I(9P) AND T(9Q18P)
    HERVA, R
    KOIVISTO, M
    [J]. HUMAN GENETICS, 1979, 50 (03) : 237 - 240
  • [6] NUMBER OF C-BANDS OF HUMAN ISOCHROMOSOME XQI AND RELATION TO 45,X-MOSAICISM
    HSU, LYF
    PACIUC, S
    DAVID, K
    CRISTIAN, S
    MOLOSHOK, R
    HIRSCHHORN, K
    [J]. JOURNAL OF MEDICAL GENETICS, 1978, 15 (03) : 222 - 226
  • [7] TRISOMY-18 SYNDROME WITH AN UNUSUAL KARYOTYPE - POSSIBLE DOUBLE ISOCHROMOSOME
    LARSON, LM
    WASDAHL, WA
    SAUMUR, JH
    COLEMAN, ML
    JALAL, SM
    [J]. JOURNAL OF MEDICAL GENETICS, 1978, 15 (01) : 73 - 76
  • [8] CHROMOSOME-15 ANOMALIES AND THE PRADER-WILLI SYNDROME - CYTOGENETIC ANALYSIS
    MATTEI, MG
    SOUIAH, N
    MATTEI, JF
    [J]. HUMAN GENETICS, 1984, 66 (04) : 313 - 334
  • [9] MUELLER HE, 1972, J MED GENET, V9, P462
  • [10] NIKAWA N, 1983, HUM GENET, V63, P85