Predictive testing for retinoblastoma comes of age

被引:22
作者
Gallie, BL [1 ]
机构
[1] HOSP SICK CHILDREN,DEPT MOL GENET,TORONTO,ON M5X 1G3,CANADA
关键词
D O I
10.1086/514861
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:279 / 281
页数:3
相关论文
共 11 条
  • [1] SPECTRUM OF GERMLINE MUTATIONS IN THE RB1 GENE - A STUDY OF 232 PATIENTS WITH HEREDITARY AND NON HEREDITARY RETINOBLASTOMA
    BLANQUET, V
    TURLEAU, C
    GROSSMORAND, MS
    BEAUFORT, CS
    DOZ, F
    BESMOND, C
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (03) : 383 - 388
  • [2] SEGREGATION ANALYSIS IN HEREDITARY RETINOBLASTOMA
    BONAITIPELLIE, C
    BRIARDGUILLEMOT, ML
    [J]. HUMAN GENETICS, 1981, 57 (04) : 411 - 419
  • [3] BREMNER R, 1997, IN PRESS AM J HUM GE
  • [4] EXPRESSION OF RECESSIVE ALLELES BY CHROMOSOMAL MECHANISMS IN RETINOBLASTOMA
    CAVENEE, WK
    DRYJA, TP
    PHILLIPS, RA
    BENEDICT, WF
    GODBOUT, R
    GALLIE, BL
    MURPHREE, AL
    STRONG, LC
    WHITE, RL
    [J]. NATURE, 1983, 305 (5937) : 779 - 784
  • [5] PATTERNS OF RISK OF HEREDITARY RETINOBLASTOMA AND APPLICATIONS TO GENETIC-COUNSELING
    DRAPER, GJ
    SANDERS, BM
    BROWNBILL, PA
    HAWKINS, MM
    [J]. BRITISH JOURNAL OF CANCER, 1992, 66 (01) : 211 - 219
  • [6] IDENTIFICATION OF GERMLINE AND SOMATIC MUTATIONS AFFECTING THE RETINOBLASTOMA GENE
    DUNN, JM
    PHILLIPS, RA
    BECKER, AJ
    GALLIE, BL
    [J]. SCIENCE, 1988, 241 (4874) : 1797 - 1800
  • [7] A HUMAN DNA SEGMENT WITH PROPERTIES OF THE GENE THAT PREDISPOSES TO RETINOBLASTOMA AND OSTEOSARCOMA
    FRIEND, SH
    BERNARDS, R
    ROGELJ, S
    WEINBERG, RA
    RAPAPORT, JM
    ALBERT, DM
    DRYJA, TP
    [J]. NATURE, 1986, 323 (6089) : 643 - 646
  • [8] SOMATIC INACTIVATION OF GENES ON CHROMOSOME-13 IS A COMMON EVENT IN RETINOBLASTOMA
    GODBOUT, R
    DRYJA, TP
    SQUIRE, J
    GALLIE, BL
    PHILLIPS, RA
    [J]. NATURE, 1983, 304 (5925) : 451 - 453
  • [10] Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma
    Lohmann, DR
    Gerick, M
    Brandt, B
    Oelschlager, U
    Lorenz, B
    Passarge, E
    Horsthemke, B
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) : 282 - 294