GENETIC IMPRINTING - DADS AND DISOMY AND DISEASE

被引:68
作者
LITTLE, M
VANHEYNINGEN, V
HASTIE, N
机构
关键词
D O I
10.1038/351609a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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页码:609 / 610
页数:2
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[1]   THE MOUSE INSULIN-LIKE GROWTH-FACTOR TYPE-2 RECEPTOR IS IMPRINTED AND CLOSELY LINKED TO THE TME LOCUS [J].
BARLOW, DP ;
STOGER, R ;
HERRMANN, BG ;
SAITO, K ;
SCHWEIFER, N .
NATURE, 1991, 349 (6304) :84-87
[2]   PARENTAL IMPRINTING OF THE MOUSE H19 GENE [J].
BARTOLOMEI, MS ;
ZEMEL, S ;
TILGHMAN, SM .
NATURE, 1991, 351 (6322) :153-155
[3]   CLINICAL AND CYTOGENETIC SURVEY OF 39 INDIVIDUALS WITH PRADER-LABHART-WILLI SYNDROME [J].
BUTLER, MG ;
MEANEY, FJ ;
PALMER, CG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) :793-809
[4]   PARENTAL IMPRINTING OF THE MOUSE INSULIN-LIKE GROWTH FACTOR-II GENE [J].
DECHIARA, TM ;
ROBERTSON, EJ ;
EFSTRATIADIS, A .
CELL, 1991, 64 (04) :849-859
[5]   EMBRYOLOGICAL AND MOLECULAR INVESTIGATIONS OF PARENTAL IMPRINTING ON MOUSE CHROMOSOME-7 [J].
FERGUSONSMITH, AC ;
CATTANACH, BM ;
BARTON, SC ;
BEECHEY, CV ;
SURANI, MA .
NATURE, 1991, 351 (6328) :667-670
[6]   UNIPARENTAL PATERNAL DISOMY IN A GENETIC CANCER-PREDISPOSING SYNDROME [J].
HENRY, I ;
BONAITIPELLIE, C ;
CHEHENSSE, V ;
BELDJORD, C ;
SCHWARTZ, C ;
UTERMANN, G ;
JUNIEN, C .
NATURE, 1991, 351 (6328) :665-667
[7]   STRUCTURAL ALTERATION OF THE INSULIN-LIKE GROWTH FACTOR-II-GENE IN WILMS TUMOR [J].
IRMINGER, JC ;
SCHOENLE, EJ ;
BRINER, J ;
HUMBEL, RE .
EUROPEAN JOURNAL OF PEDIATRICS, 1989, 148 (07) :620-623
[8]   ANGELMAN AND PRADER-WILLI SYNDROMES SHARE A COMMON CHROMOSOME-15 DELETION BUT DIFFER IN PARENTAL ORIGIN OF THE DELETION [J].
KNOLL, JHM ;
NICHOLLS, RD ;
MAGENIS, RE ;
GRAHAM, JM ;
LALANDE, M ;
LATT, SA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (02) :285-290
[9]   MOLECULAR NATURE OF GENETIC CHANGES RESULTING IN LOSS OF HETEROZYGOSITY OF CHROMOSOME-11 IN WILMS-TUMORS [J].
MANNENS, M ;
SLATER, RM ;
HEYTING, C ;
BLIEK, J ;
DEKRAKER, J ;
COAD, N ;
DEPAGTERHOLTHUIZEN, P ;
PEARSON, PL .
HUMAN GENETICS, 1988, 81 (01) :41-48
[10]   GENETIC IMPRINTING SUGGESTED BY MATERNAL HETERODISOMY IN NONDELETION PRADER-WILLI SYNDROME [J].
NICHOLLS, RD ;
KNOLL, JHM ;
BUTLER, MG ;
KARAM, S ;
LALANDE, M .
NATURE, 1989, 342 (6247) :281-285