首页> 外文OA文献 >Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia

【2h】

Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia

机译：Cryptic t（19; 19）（p13.3; q13.2），涉及TCF3 / E2a基因，通过分子细胞遗传学在儿童B细胞祖细胞急性淋巴细胞白血病患者中检测和描述

页面导航

摘要
著录项
相似文献
相关主题

摘要

Case report on a case of cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia.

机译：一例涉及TCF3 / E2A基因的秘密t（19; 19）（p13.3; q13.2）病例报告，通过分子细胞遗传学方法在一名儿童B细胞祖细胞急性淋巴细胞白血病患者中进行了检测和描述。

著录项

作者
Ney Garcia DR; Vieira TP; Liehr T; Abdelhay E; Binato R; Neves F; de Souza MT; Ribeiro RC; Silva MLM;
展开▼
作者单位

展开▼
年度 2014
总页数
原文格式 PDF
正文语种 en
中图分类

相似文献

外文文献
中文文献
专利

1. Allogeneic hematopoietic stem cell transplantation for adult patients with B-cell acute lymphoblastic leukemia harboring t(1;19)(q23;p13.3); comparison with normal karyotype [J] . Bone marrow transplantation . 2020,第7期

机译：异种造血干细胞移植成年患者患有T（1; 19）的B细胞急性淋巴细胞白血病（Q23; P13.3）; 与正常核型进行比较
2. A complex 1;19;11 translocation involving the MLL gene in a patient with congenital acute monoblastic leukemia identified by molecular and cytogenetic techniques. [J] . De Braekeleer E, Meyer C, Douet Guilbert N Annals of hematology . 2009,第8期

机译：通过分子和细胞遗传学技术鉴定的先天性急性单细胞白血病患者中涉及MLL基因的复杂的1; 19; 11易位。
3. A complex 1;19;11 translocation involving the MLL gene in a patient with congenital acute monoblastic leukemia identified by molecular and cytogenetic techniques [J] . Etienne De Braekeleer, Claus Meyer, Nathalie Douet-Guilbert, Annals of Hematology . 2009,第8期

机译：通过分子和细胞遗传学技术鉴定的先天性急性单细胞白血病患者中涉及MLL基因的复杂1; 19; 11易位
4. Machine Learning Approach to Predict the Survival Time of Childhood Acute Lymphoblastic Leukemia Patients [C] . Rangana Jayashanka, C.R. Wijesinghe, A.R. Weerasinghe, International Conference on Advances in ICT for Emerging Regions . 2018

机译：机器学习方法预测儿童急性淋巴细胞白血病患者的生存时间
5. Evidence for heterogeneous genetic associations with acute lymphoblastic leukemia (ALL) by cytogenetics, age, and sex in high-risk patients treated with matched unrelated donor allogeneic blood or marrow transplant (URD-BMT) [D] . Clay, Alyssa I. 2016

机译：通过匹配的无关供体同种异体造血或骨髓移植（URD-BMT）治疗的高危患者中，通过细胞遗传学，年龄和性别进行的与急性淋巴细胞白血病（ALL）异质遗传关联的证据
6. Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1 6 and 13: a case report [O] . Abdulsamad Wafa, Manar As’sad, Thomas Liehr, 2017

机译：儿童易位t（1; 19）（q21.1; p13.3）的B前急性淋巴细胞性白血病和另外两个涉及染色体1、6和13的染色体畸变：一例
7. Molecular cytogenetics characterization of a novel translocation involving chromosomes 17 and 19 in a Ph+ adult acute lymphoblastic leukemia [O] . G. SPECCHIA, ALBANO F, L.ANELLI, 2002

机译：Ph +成人急性淋巴细胞白血病中涉及染色体17和19的新型易位的分子细胞遗传学表征

Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia

摘要

著录项

相似文献

相关主题

期刊订阅