X-linked Wiskott-Aldrich syndrome in a girl

被引：79
作者：
Parolini, O
Ressmann, G
Haas, OA
Pawlowsky, J
Gadner, H
Knapp, W
Holter, W
机构：
[1] Univ Vienna, NFI, Inst Immunol VIRCC, A-1235 Vienna, Austria
[2] St Anna Childrens Hosp, A-1090 Vienna, Austria
来源：
NEW ENGLAND JOURNAL OF MEDICINE | 1998年 / 338卷 / 05期
关键词：
D O I：
10.1056/NEJM199801293380504
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：291 / 295
页数：5
相关论文
共 28 条
[1]  
ALLEN RC, 1992, AM J HUM GENET, V51, P1229
[2]  
Aral B, 1996, HUM MUTAT, V7, P52, DOI 10.1002/(SICI)1098-1004(1996)7:1<52::AID-HUMU7>3.3.CO
[3]  
2-0
[4]   X-CHROMOSOME METHYLATION IN MANIFESTING AND HEALTHY CARRIERS OF DYSTROPHINOPATHIES - CONCORDANCE OF ACTIVATION RATIOS AMONG FIRST DEGREE FEMALE RELATIVES AND SKEWED INACTIVATION AS CAUSE OF THE AFFECTED PHENOTYPES [J].
AZOFEIFA, J ;
VOIT, T ;
HUBNER, C ;
CREMER, M .
HUMAN GENETICS, 1995, 96 (02) :167-176
[5]  
Belmont JW, 1996, AM J HUM GENET, V58, P1101
[6]  
CLARKE JTR, 1991, AM J HUM GENET, V49, P289
[7]  
CONLEY ME, 1992, BLOOD, V80, P1264
[8]  
DERRY JM, 1994, CELL, V79, pA922
[9]   ISOLATION OF A NOVEL GENE MUTATED IN WISKOTT-ALDRICH SYNDROME [J].
DERRY, JMJ ;
OCHS, HD ;
FRANCKE, U .
CELL, 1994, 78 (04) :635-644
[10]  
FEARON ER, 1988, BLOOD, V72, P1735
123