Chromosome studies in potentially leukaemic myeloid disorders.
作者信息
Jensen M K
出版信息
Acta Med Scand. 1968 Jun;183(6):535-42. doi: 10.1111/j.0954-6820.1968.tb10519.x.
Abstract
摘要
相似文献
1
Chromosome studies in potentially leukaemic myeloid disorders.
Acta Med Scand. 1968 Jun;183(6):535-42. doi: 10.1111/j.0954-6820.1968.tb10519.x.
2
[Chronic myeloproliferative diseases. Clinical and cytogenetic study].[慢性骨髓增殖性疾病。临床与细胞遗传学研究]
Sangre (Barc). 1971;16(2):159-84.
3
Specificity of the Ph1 chromosome.Ph1染色体的特异性
Lancet. 1967 Dec 16;2(7529):1312-3. doi: 10.1016/s0140-6736(67)90429-1.
4
Acquired partial deletions of the long arm of chromosome 5 in hematologic disorders.血液系统疾病中获得性5号染色体长臂部分缺失
Am J Hematol. 1983 Nov;15(3):295-310. doi: 10.1002/ajh.2830150311.
5
Duplication of part of chromosome no. 1 in myeloproliferative diseases.骨髓增殖性疾病中1号染色体部分片段的重复。
Lancet. 1978 Jan 14;1(8055):96-7. doi: 10.1016/s0140-6736(78)90032-6.
6
Leukaemia cytogenetics.白血病细胞遗传学
Med J Aust. 1975 Apr 19;1(16):495-9.
7
Chromosomal abnormalities in human neoplasia.人类肿瘤中的染色体异常。
Annu Rev Med. 1970;21:379-408. doi: 10.1146/annurev.me.21.020170.002115.
8
9
10
[Cytogenetics and hemopathies].[细胞遗传学与血液病]
Nouv Rev Fr Hematol. 1972 Jul-Aug;12(4):510-5.
引用本文的文献
1
The occurrence of the philadelphia chromosome in essential thrombocytosis.原发性血小板增多症中费城染色体的出现。
Hum Genet. 1981;56(3):287-91. doi: 10.1007/BF00274681.
2
[Anusual chromosome set (46,XX,Dq-) in osteomyelofibrosis].
Blut. 1974 Jun;28(6):411-4. doi: 10.1007/BF01630104.
3
Familial acute myeloid leukaemia with acquired Pelger-Huet anomaly and aneuploidy of C group.伴有获得性Pelger-Huet异常和C组非整倍体的家族性急性髓系白血病。
Br Med J. 1972 Nov 11;4(5836):327-31. doi: 10.1136/bmj.4.5836.327.
Zotero 插件