• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia.

作者信息

Huret J L, Benz E, Guilhot F, Brizard A, Tanzer J

出版信息

Hum Genet. 1986 Sep;74(1):98-100. doi: 10.1007/BF00278794.

DOI:10.1007/BF00278794
PMID:3759089
Abstract

A 10-year-old Fanconi anaemia patient showed a 46,XX/46,XX,-7,+i(7q) constitution in bone marrow which disappeared without any specific treatment and then reappeared during a year of survey. We discuss i(7q) and Fanconi anaemia.

摘要

相似文献

1
Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia.
Hum Genet. 1986 Sep;74(1):98-100. doi: 10.1007/BF00278794.
2
Karyotype evolution in the bone marrow of a patient with Fanconi anemia: breakpoints in clonal anomalies of this disease.
Cytogenet Cell Genet. 1988;48(4):224-7. doi: 10.1159/000132633.
3
Myelodysplastic syndrome with trisomy 8 in an adolescent with Fanconi anaemia and selective IgA deficiency.
Am J Hematol. 1989 Aug;31(4):280-3. doi: 10.1002/ajh.2830310413.
4
[Fanconi's anemia: chromosome anormalies].
Sem Hop. 1976 Dec;52(44):2505-12.
5
Chromosome abnormalities in bone marrow of Fanconi anemia patients.范可尼贫血患者骨髓中的染色体异常。
Cancer Genet Cytogenet. 1993 Jan;65(1):47-50. doi: 10.1016/0165-4608(93)90057-s.
6
[Karyotype of peripheral blood and bone marrow cells in Fanconi's anaemia (author's transl)].范科尼贫血患者外周血及骨髓细胞的核型（作者译）
Bratisl Lek Listy. 1977 Oct;68(4):424-35.
7
[Cytogenetic studies in four cases of Fanconi's anemia (author's transl)].
Nouv Rev Fr Hematol. 1975 Sep-Oct;15(5):539-50.
8
Fanconi anaemia--constitutional, familial aplastic anaemia.
Baillieres Clin Haematol. 1989 Jan;2(1):139-52. doi: 10.1016/s0950-3536(89)80011-3.
9
A spontaneous clone of Fanconi anemia fibroblasts with chromosome abnormalities and increased growth potential.
Cytogenet Cell Genet. 1980;28(4):265-70. doi: 10.1159/000131539.
10
Fanconi's anaemia; chromosome breakage in a large African family.
Hereditas. 1980;93(2):255-60. doi: 10.1111/j.1601-5223.1980.tb01365.x.

本文引用的文献

1
Similar chromosomal abnormalities in several retinoblastomas.多个视网膜母细胞瘤中存在相似的染色体异常。
Hum Genet. 1982;61(3):201-4. doi: 10.1007/BF00296442.
2
An analysis of chromosome findings in non-Hodgkin's lymphomas.非霍奇金淋巴瘤染色体检查结果分析
Cancer Genet Cytogenet. 1982 Feb;5(2):107-21. doi: 10.1016/0165-4608(82)90002-4.
3
4;11 translocation in acute lymphoblastic leukemia: a specific syndrome.急性淋巴细胞白血病中的4;11易位：一种特殊综合征。
Cancer Genet Cytogenet. 1982 Oct;7(2):165-72. doi: 10.1016/0165-4608(82)90012-7.
4
Acute leukemia associated with the t(4;11) chromosome rearrangement: ultrastructural and immunologic characteristics.与t(4;11)染色体重排相关的急性白血病：超微结构和免疫学特征
Blood. 1982 Dec;60(6):1321-31.
5
Translocation 4; 11 in acute lymphoblastic leukemia: clinical characteristics and prognostic significance.急性淋巴细胞白血病中的4号与11号染色体易位：临床特征及预后意义
Blood. 1982 Jan;59(1):96-9.
6
Chromosomal studies of leukemic and preleukemic Fanconii's anemia patients: examples of acquired 'chromosomal amplification.'.
Hum Genet. 1980;56(1):59-62. doi: 10.1007/BF00281569.
7
Lymphoblastic lymphoma: cytogenetic, pathologic, and immunologic studies.
Int J Cancer. 1982 Sep 15;30(3):273-9. doi: 10.1002/ijc.2910300304.
8
Transformation of Fanconi's anemia to acute nonlymphocytic leukemia associated with emergence of monosomy 7.范可尼贫血转化为急性非淋巴细胞白血病并伴有7号染色体单体的出现。
Blood. 1984 Jul;64(1):173-6.
9
Familial leukemia and aplastic anemia associated with monosomy 7.
Am J Med. 1983 Nov;75(5):756-62. doi: 10.1016/0002-9343(83)90404-7.
10
[Burkitt's acute lymphoblastic leukemia. Incidence and cytogenetic aspects].[伯基特急性淋巴细胞白血病。发病率及细胞遗传学方面]
Nouv Rev Fr Hematol (1978). 1983;25(5):303-9.