Acquired elliptocytosis in a patient with a myelodysplastic syndrome associated with 20q deletion

Quiroz‐Cervantes Keina S.; Juárez‐Salcedo Luis Miguel; Nuevo Irene; Guillén Helga; Arbeteta Jaime; Golbano Nuria

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Acquired elliptocytosis in a patient with a myelodysplastic syndrome associated with 20q deletion

机译：在患者中获得骨髓细胞增多症，其肌小型增生综合征与20Q缺失相关

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来源
《British Journal of Haematology》 |2019年第2期|共1页
作者
Quiroz‐Cervantes Keina S.; Juárez‐Salcedo Luis Miguel; Nuevo Irene; Guillén Helga; Arbeteta Jaime; Golbano Nuria;
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作者单位

Department of Malignant HematologyUniversity Hospital of GuadalajaraCastilla‐La Mancha Spain;

Department of Malignant HematologyUniversity Hospital of GuadalajaraCastilla‐La Mancha Spain;

Department of Malignant HematologyUniversity Hospital of GuadalajaraCastilla‐La Mancha Spain;

Department of Malignant HematologyUniversity Hospital of GuadalajaraCastilla‐La Mancha Spain;

Department of Malignant HematologyUniversity Hospital of GuadalajaraCastilla‐La Mancha Spain;

Department of Malignant HematologyUniversity Hospital of GuadalajaraCastilla‐La Mancha Spain;

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正文语种 eng
中图分类血液及淋巴系疾病;
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1. Acquired elliptocytosis in a patient with a myelodysplastic syndrome associated with 20q deletion [J] . Quiroz‐Cervantes Keina S., Juárez‐Salcedo Luis Miguel, Nuevo Irene, British Journal of Haematology . 2019,第2期

机译：在患者中获得骨髓细胞增多症，其肌小型增生综合征与20Q缺失相关
2. Protein 4.1 deficiency and deletion of chromosome 20q are associated with acquired elliptocytosis in myelodysplastic syndrome. [J] . Hur M, Lee KM, Cho HC, Clinical and laboratory haematology . 2004,第1期

机译：蛋白4.1缺乏和20q染色体缺失与骨髓增生异常综合症中获得性卵白细胞增多有关。
3. Investigation of 305 patients with myelodysplastic syndromes and 20q deletion for associated cytogenetic and molecular genetic lesions and their prognostic impact [J] . BacherU., HaferlachT., SchnittgerS., British Journal of Haematology . 2014,第6期

机译：305例骨髓增生异常综合征和20q缺失伴发细胞遗传学和分子遗传学损害的患者及其预后影响的调查
4. Acquired Glanzmann Thrombasthenia in a Patient with Myelodysplastic Syndrome [C] . A. Trummer, A. Tiede, R. Eisert Hemophilia Symposium . 2008

机译：在患有髓细胞增强综合征的患者中获得了Glanzmann血栓血管瘤
5. Chromosomal mapping of genes encoding human Pur-alpha and Pur-beta: Independent and simultaneous deletions in myelodysplastic syndromes and acute myelogenous leukemia. [D] . Lezon-Geyda, Kimberly Ann. 2001

机译：编码人Pur-alpha和Pur-beta的基因的染色体作图：骨髓增生异常综合症和急性骨髓性白血病的独立和同时缺失。
6. Acquired Elliptocytosis as a Manifestation of Myelodysplastic Syndrome Associated with Deletion of Chromosome 20q [O] . Sukesh Manthri, Naresh K. Vasireddy, Sindhura Bandaru, 2018

机译：获得性细胞增多症表现为与20q染色体缺失相关的骨髓增生异常综合症
7. Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes [O] . FA Asimakopoulos, TL Holloway, EP Nacheva, 1996

机译：检测骨髓间隙中染色体20Q缺失，但不含髓原障碍患者的外周血粒细胞或髓细胞异常综合征

Acquired elliptocytosis in a patient with a myelodysplastic syndrome associated with 20q deletion

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