Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia

被引:5
作者
Goehring, G.
Hanke, C.
Kratz, C.
Kontny, U.
Steinemann, D.
Niemeyer, C. M.
Schlegelberger, B.
机构
[1] Hannover Med Sch, Inst Cell & Mol Pathol, D-30625 Hannover, Germany
[2] Univ Freiburg, Dept Pediat, Div Pediat Hematol & Oncol, D-7800 Freiburg, Germany
关键词
D O I
10.1007/s00277-006-0177-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:883 / 885
页数:3
相关论文
共 7 条
[1]   Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24) [J].
Gadzicki, D. ;
Baumer, A. ;
Wey, E. ;
Happel, C. M. ;
Rudolph, C. ;
Onnies, H. T. R. ;
Neitzel, H. ;
Steinemann, D. ;
Welte, K. ;
Klein, C. ;
Schlegelberger, B. .
ANNALS OF HUMAN GENETICS, 2006, 70 :958-964
[2]  
Gangarossa S, 1996, AM J MED GENET, V62, P120, DOI 10.1002/(SICI)1096-8628(19960315)62:2<120::AID-AJMG4>3.0.CO
[3]  
2-#
[4]  
Germeshausen Manuela, 2006, Hum Mutat, V27, P296, DOI 10.1002/humu.9415
[5]   The 11q terminal deletion disorder: A prospective study of 110 cases [J].
Grossfeld, PD ;
Mattina, T ;
Lai, Z ;
Favier, R ;
Jones, KL ;
Cotter, F ;
Jones, C .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 129A (01) :51-61
[6]  
PENNY LA, 1995, AM J HUM GENET, V56, P676
[7]  
Tunnacliffe A, 1999, GENOME RES, V9, P44