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Myeloproliferative Disorder with Unusual Marrow Chromosome Constitution

机译：具有异常骨髓染色体组成的骨髓增生性疾病

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作者
Whaun, J. M.; Lin, C. C.; Biederman, B.; Cornish, S. J.; Dundas, J. B.;
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年度 1980
页码 p.1-7
总页数 7
原文格式 PDF
正文语种 eng
中图分类工业技术;
关键词
Bone marrow; Chromosomes; Diseases; Case studies; Patients; Hematology; Reprints;

机译：骨髓;染色体;疾病;病例研究;患者;血液学;重印;

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专利

1. Bone marrow CD34+ progenitor cells in Philadelphia chromosome-negative chronic myeloproliferative disorders--a clinicopathological study on 575 patients. [J] . Thiele J, Kvasnicka HM, Diehl V Leukemia and lymphoma . 2005,第5期

机译：费城染色体阴性慢性骨髓增生性疾病中的骨髓CD34 +祖细胞-575名患者的临床病理研究。
2. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions. [J] . De-Braekeleer M Annals of hematology . 2008,第7期

机译：骨髓增生异常综合症和费城染色体阴性的骨髓增生性疾病中的20号染色体缺失：通过分子细胞遗传学鉴定通常缺失和保留的区域。
3. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions [J] . Nathalie Douet-Guilbert, Audrey Basinko, Frédéric Morel, Annals of Hematology . 2008,第7期

机译：骨髓增生异常综合症和费城染色体阴性的骨髓增生性疾病中的20号染色体缺失：通过分子细胞遗传学鉴定通常缺失和保留的区域
4. Identification of JAK2V617F Mutation on Myeloproliferative Disorders in Medan [C] . Dwi Rita Anggraini, Hidayat, Mega Sari Sitorus Public Health International Conference . 2017

机译：尼曼野生鳞型疾病鉴定JAK2V617F突变
5. A genetic association study of reading disabilities and attention deficit hyperactivity disorder with a candidate region on chromosome 6p and a gene on chromosome 1p [D] . Couto, Jillian Michelle 2008

机译：阅读障碍和注意力缺陷多动障碍的遗传关联研究，其候选区域位于6p号染色体上，而一个基因位于1p号染色体上
6. The Chromosome Constitution of Human Marrow in Various Developmental and Blood Disorders [O] . Avery A. Sandberg, George F. Koepf, Lois H. Crosswhite, 1960

机译：各种发育和血液疾病中骨髓的染色体组成
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

Myeloproliferative Disorder with Unusual Marrow Chromosome Constitution

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