学术探索
学术期刊
新闻热点
数据分析
智能评审

TRANS-SENSING HYPOTHESIS FOR ORIGIN OF BECKWITH-WIEDEMANN SYNDROME

被引：11
作者：
FIDLER, AE
MAW, MA
ECCLES, MR
REEVE, AE
机构：
来源：
LANCET | 1992年 / 339卷 / 8787期
关键词：
D O I：
10.1016/0140-6736(92)90042-2
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：243 / 243
页数：1
相关论文
共 10 条
  • [1] PARENTAL IMPRINTING OF THE MOUSE INSULIN-LIKE GROWTH FACTOR-II GENE
    DECHIARA, TM
    ROBERTSON, EJ
    EFSTRATIADIS, A
    [J]. CELL, 1991, 64 (04) : 849 - 859
  • [2] EMBRYOLOGICAL AND MOLECULAR INVESTIGATIONS OF PARENTAL IMPRINTING ON MOUSE CHROMOSOME-7
    FERGUSONSMITH, AC
    CATTANACH, BM
    BARTON, SC
    BEECHEY, CV
    SURANI, MA
    [J]. NATURE, 1991, 351 (6328) : 667 - 670
  • [3] CHROMOSOME-11 UNIPARENTAL ISODISOMY PREDISPOSING TO EMBRYONAL NEOPLASMS
    GRUNDY, P
    TELZEROW, P
    PATERSON, MC
    HABER, D
    BERMAN, B
    LI, F
    GARBER, J
    [J]. LANCET, 1991, 338 (8774) : 1079 - 1080
  • [4] MOLECULAR DEFINITION OF THE 11P15.5 REGION INVOLVED IN BECKWITH-WIEDEMANN SYNDROME AND PROBABLY IN PREDISPOSITION TO ADRENOCORTICAL CARCINOMA
    HENRY, I
    JEANPIERRE, M
    COUILLIN, P
    BARICHARD, F
    SERRE, JL
    JOURNEL, H
    LAMOUROUX, A
    TURLEAU, C
    DEGROUCHY, J
    JUNIEN, C
    [J]. HUMAN GENETICS, 1989, 81 (03) : 273 - 277
  • [5] UNIPARENTAL PATERNAL DISOMY IN A GENETIC CANCER-PREDISPOSING SYNDROME
    HENRY, I
    BONAITIPELLIE, C
    CHEHENSSE, V
    BELDJORD, C
    SCHWARTZ, C
    UTERMANN, G
    JUNIEN, C
    [J]. NATURE, 1991, 351 (6328) : 665 - 667
  • [6] GENETIC IMPRINTING - DADS AND DISOMY AND DISEASE
    LITTLE, M
    VANHEYNINGEN, V
    HASTIE, N
    [J]. NATURE, 1991, 351 (6328) : 609 - 610
  • [7] MANNENS M, 1991, AM J HUM GENET S, V49, P149
  • [8] GENOMIC IMPRINTING IN MAMMALIAN DEVELOPMENT - A PARENTAL TUG-OF-WAR
    MOORE, T
    HAIG, D
    [J]. TRENDS IN GENETICS, 1991, 7 (02) : 45 - 49
  • [9] TRANS-SENSING EFFECTS FROM DROSOPHILA TO HUMANS
    TARTOF, KD
    HENIKOFF, S
    [J]. CELL, 1991, 65 (02) : 201 - 203
  • [10] MOLECULAR CHARACTERIZATION OF BECKWITH-WIEDEMANN SYNDROME (BWS) PATIENTS WITH PARTIAL DUPLICATION OF CHROMOSOME-11P EXCLUDES THE GENE MYOD1 FROM THE BWS REGION
    WEKSBERG, R
    GLAVES, M
    TESHIMA, I
    WAZIRI, M
    PATIL, S
    WILLIAMS, BRG
    [J]. GENOMICS, 1990, 8 (04) : 693 - 698
1