GENOMIC IMPRINTING AND GENETIC-DISORDERS IN MAN

被引:146
作者
REIK, W
机构
关键词
D O I
10.1016/0168-9525(89)90138-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:331 / 336
页数:6
相关论文
共 40 条
[1]  
AGULNIK AI, 1988, MOUSE NEWS LETT, V81, P77
[2]   UNMASKING MOLES [J].
BAGSHAWE, KD ;
LAWLER, SD .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1982, 89 (04) :255-257
[3]  
CATTANACH BM, 1986, J EMBRYOL EXP MORPH, V97, P137
[4]  
CATTANACH BM, 1988, MOUSE NEWSLETTER, V82, P93
[5]   ALLELE-SPECIFIC METHYLATION OF THE HUMAN C-HA-RAS-1 GENE [J].
CHANDLER, LA ;
GHAZI, H ;
JONES, PA ;
BOUKAMP, P ;
FUSENIG, NE .
CELL, 1987, 50 (05) :711-717
[6]   PARENTAL ORIGIN OF MUTATIONS OF THE RETINOBLASTOMA GENE [J].
DRYJA, TP ;
MUKAI, S ;
PETERSEN, R ;
RAPAPORT, JM ;
WALTON, D ;
YANDELL, DW .
NATURE, 1989, 339 (6225) :556-558
[7]  
Eldridge R, 1981, Adv Neurol, V29, P57
[8]   The experimental modification of dominance in Danforth's short-tailed mutant mice [J].
Fisher, RA ;
Holt, SB .
ANNALS OF EUGENICS, 1943, 12 :102-120
[9]   HUNTINGTONS-DISEASE - 2 FAMILIES WITH DIFFERING CLINICAL-FEATURES SHOW LINKAGE TO THE G8 PROBE [J].
FOLSTEIN, SE ;
PHILLIPS, JA ;
MEYERS, DA ;
CHASE, GA ;
ABBOTT, MH ;
FRANZ, ML ;
WABER, PG ;
KAZAZIAN, HH ;
CONNEALLY, PM ;
HOBBS, W ;
TANZI, R ;
FARYNIARZ, A ;
GIBBONS, K ;
GUSELLA, J .
SCIENCE, 1985, 229 (4715) :776-779
[10]  
GREGER V, IN PRESS HUM GENET