Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation

被引:143
作者
Thompson, AA [1 ]
Nguyen, LT [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Pediat, Div Hematol Oncol,Gwynne Hazen Cherry Mem Labs, Los Angeles, CA 90024 USA
关键词
D O I
10.1038/82511
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:397 / 398
页数:2
相关论文
共 15 条
[11]   Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 [J].
Muragaki, Y ;
Mundlos, S ;
Upton, J ;
Olsen, BR .
SCIENCE, 1996, 272 (5261) :548-551
[12]   Genetic interactions of Hox genes in limb development: learning from compound mutants [J].
Rijli, FM ;
Chambon, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1997, 7 (04) :481-487
[13]  
SCHROEDERKURTH TM, 1989, FANCONI ANEMIA CLIN, P264
[14]   HOMEOTIC TRANSFORMATIONS AND LIMB DEFECTS IN HOX-A11 MUTANT MICE [J].
SMALL, KM ;
POTTER, SS .
GENES & DEVELOPMENT, 1993, 7 (12A) :2318-2328
[15]   Overexpression of HOXA10 in murine hematopoietic cells perturbs both myeloid and lymphoid differentiation and leads to acute myeloid leukemia [J].
Thorsteinsdottir, U ;
Sauvageau, G ;
Hough, MR ;
Dragowska, W ;
Lansdorp, PM ;
Lawrence, HJ ;
Largman, C ;
Humphries, RK .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (01) :495-505