نتایج جستجو برای: q22

تعداد نتایج: 928  

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2008
Francois M Cady Brian Patrick O'Neill Mark E Law Paul A Decker David M Kurtz Caterina Giannini Alyx B Porter Paul J Kurtin Patrick B Johnston Ahmet Dogan Ellen D Remstein

PURPOSE Primary CNS lymphoma (PCNSL) is an aggressive lymphoma but clinically validated biologic markers that can predict natural history to tailor treatment according to risk are lacking. Several genetic changes including BCL6 rearrangements and deletion of 6q22, containing the putative tumor suppressor gene PTPRK, are potential risk predictors. Herein we determined the prevalence and survival...

Journal: :Haematologica 2005
Zhijian Xiao Shihe Liu Xuping Liu Minghua Yu Yushu Hao

We report on 6 patients with tetraploidy or near-tetraploidy acute myeloid leukemia (AML) with double t(8;21) (q22;q22) and review the literature on cases with the same cytogenetic abnormalities. Some common features were revealed by this analysis.

Journal: :Haematologica 1999
S Siena G Sammarelli M G Grimoldi R Schiavo A Nozza M Roncalli C Mecucci A Santoro C Carlo-Stella

We report a new chromosomal reciprocal translocation t(5;10)(q33;q22) in a 49-year-old man with atypical chronic myeloid leukemia (a-CML) and history of occupational exposure to petroleum products including benzene and other hydrocarbons. The t(5;10) (q33;q22) was found in 94% and 84% of metaphases in peripheral blood and bone marrow cells, respectively. Cytogenetic analysis of single colonies ...

Journal: :Genetics and molecular research : GMR 2010
P Burégio-Frota L Valença G F Leal A R Duarte A V S Bispo-Brito E M Soares-Ventura T J Marques-Salles M T M C Nogueira M T C Muniz M L M Silva F Hunstig T Liehr N Santos

We report on a 23-year-old girl with short stature, short and wide neck, low posterior hairline, hypogonadism, underdeveloped breasts, infantile uterus, ovaries not visualized, and primary amenorrhea. Cytogenetic G-banding analysis revealed a mosaic karyotype of 46,X,dup(X)(q22)[35]/45,X[15], confirming the clinical suspicion of Turner syndrome. Molecular cytogenetics using a multicolor banding...

Journal: :Oncology letters 2015
Zhifen Zhang Jianwen Zou Yuantang Li Zhanfeng Liu Rui Xu Wenjun Tian Zongchen Zhao Hui Sun Jingying Han Jia Wang Bingchang Zhang Ying Ju

The present study reviewed three patients with acute myeloid leukemia (AML) who had the specific genetic abnormality t(16;21)(p11;q22). To investigate the clinical and laboratory characteristics of AML with t(16;21)(p11;q22) translocation, the similarities and differences of clinical characteristics and laboratory examinations were compared, and a literature review was conducted. According to t...

Journal: :American Journal of Clinical Pathology 2004

Journal: :Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion 2011
Guillermo J Ruiz-Delgado Julio Macías-Gallardo Julia Lutz-Presno Javier Garcés-Eisele Ana Hernández-Arizpe Maryel Montes-Montiel Guillermo J Ruiz-Argüelles

Twenty one patients with CBF-AML presented prospectively in the Centro de Hematología y Medicina Interna de Puebla (Puebla, México) between February 1995 and March 2010, 14 with the t(8;21)(q22;q22) and 7 with the inv(16)(p13;q22)/t(16;16)(p13;q22); they represent 13% of all cases of AML. The median age of the patients was 24 years (range 1 to 61). Seven of 14 patients with t(8;21)(q22;q22) had...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

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