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Clonal occurrence of a chromosome Dq--in myelosclerosis with myeloid metaplasia.

作者信息

Engel W, Merker H, Schneider G, Wolf U

出版信息

Humangenetik. 1968;6(4):335-7. doi: 10.1007/BF00286802.

DOI:10.1007/BF00286802
PMID:5713619
Abstract
摘要

相似文献

1
Clonal occurrence of a chromosome Dq--in myelosclerosis with myeloid metaplasia.骨髓化生伴骨髓纤维化中染色体Dq--的克隆性出现。
Humangenetik. 1968;6(4):335-7. doi: 10.1007/BF00286802.
2
Isochromosome 17q in a case of myelofibrosis with myeloid metaplasia terminating in blastic transformation.
Cancer Genet Cytogenet. 1987 Feb;24(2):221-4. doi: 10.1016/0165-4608(87)90102-6.
3
Multiple active X chromosomes in myelofibrosis with myeloid metaplasia.
Cancer Genet Cytogenet. 1981 Mar;3(2):137-44. doi: 10.1016/0165-4608(81)90068-6.
4
Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia.
Cancer Genet Cytogenet. 2002 Aug;137(1):68-71. doi: 10.1016/s0165-4608(02)00554-x.
5
Cytogenetic studies in twelve patients with primary myelofibrosis and myeloid metaplasia.对12例原发性骨髓纤维化和髓样化生患者的细胞遗传学研究。
Cancer Genet Cytogenet. 1987 Jan;24(1):151-8. doi: 10.1016/0165-4608(87)90092-6.
6
Cytogenetics of acute and chronic myelofibrosis.急性和慢性骨髓纤维化的细胞遗传学
Virchows Arch B Cell Pathol. 1978 Nov 17;29(1-2):45-50. doi: 10.1007/BF02899335.
7
Abnormalities of chromosome 13 in myelofibrosis.
Scand J Haematol. 1984 Jul;33(1):15-21. doi: 10.1111/j.1600-0609.1984.tb02204.x.
8
Group C monosomy in myelofibrosis with myeloid metaplasia.骨髓纤维化伴髓外化生中的C组染色体单体。
Arch Intern Med. 1967 Apr;119(4):403-6.
9
[A cytogenetical study of chronic myeloid leukemia, osteomyelosclerosis, myelofibrosis and erythrema].
Tsitologiia. 1966 Mar-Apr;8(2):229-40.
10
[An autopsy case of myelofibrosis with myeloid metaplasia terminating in blastic transformation with chromosomal aberration (i(17q))].[一例伴有髓外化生的骨髓纤维化尸检病例，最终发展为伴有染色体畸变（i(17q)）的原始细胞转化]
Rinsho Ketsueki. 1984 Jun;25(6):864-9.

引用本文的文献

1
Cytogenetic studies on mid-trimester abortuses.孕中期流产儿的细胞遗传学研究。
Humangenetik. 1970;10(4):273-97. doi: 10.1007/BF00278765.
2
Letter: Acute myelofibrosis and chromosome damage after procarbazine treatment.信函：丙卡巴肼治疗后的急性骨髓纤维化和染色体损伤
Br Med J. 1974 Aug 24;3(5929):525. doi: 10.1136/bmj.3.5929.525-b.

本文引用的文献

1
Comparison of chromosome constitution in chronic myelocytic leukemia and other myeloproliferative disorders.
Blood. 1962 Oct;20:393-423.
2
GROUP-C TRISOMY IN MYELOID METAPLASIA WITH POSSIBLE LEUKEMIA.伴有可能白血病的骨髓化生中的C组三体性
Blood. 1964 Dec;24:716-25.
3
Chromosome studies in preleukemia. I. Aneuploidy of group C chromosomes in three patients.
Blood. 1966 Jun;27(6):782-99.
4
The chromosomes in polycythaemia vera.
Br J Haematol. 1966 Sep;12(5):507-28. doi: 10.1111/j.1365-2141.1966.tb00134.x.
5
[Chromosome anomaly in a case of erythroleukemic syndrome].[一例红白血病综合征患者的染色体异常]
Prog Med (Napoli). 1965 May 31;21(10):309-17.
6
[Chromosome translocation in chronic myeloproliferative syndrome. Report on 2 observations with special reference to pathogenetic viewpoints].[慢性骨髓增殖综合征中的染色体易位。关于2例观察报告并特别提及发病机制观点]
Klin Wochenschr. 1968 Jun 1;46(11):593-600. doi: 10.1007/BF01747839.
7
Chromosomal studies in erythroleukemia and chronic erythremic myelosis.红白血病和慢性红细胞增多性骨髓化生的染色体研究
Blood. 1968 Feb;31(2):202-15.
8
Models for clonal evolutions: a study of chronic myelogenous leukemia.克隆进化模型：慢性粒细胞白血病的一项研究
Am J Hum Genet. 1966 Sep;18(5):485-503.
9
Cytogenetic studies in the chronic myeloproliferative syndrome.
Blood. 1966 Aug;28(2):241-52.
10
A constant chromosome aberration in two children with acute myeloic leukaemia.两名急性髓细胞白血病患儿存在恒定的染色体畸变。
Humangenetik. 1967 Nov 29;5(1):80-2. doi: 10.1007/BF00286218.