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Identification of translocation chromosomes by quinacrine fluorescence.

作者信息

Breg W R, Miller D A, Allderdice P W, Miller O J

出版信息

Am J Dis Child. 1972 Jun;123(6):561-4. doi: 10.1001/archpedi.1972.02110120085007.

DOI:10.1001/archpedi.1972.02110120085007
PMID:4113489
Abstract
摘要

相似文献

1
Identification of translocation chromosomes by quinacrine fluorescence.用喹吖因荧光法鉴定易位染色体。
Am J Dis Child. 1972 Jun;123(6):561-4. doi: 10.1001/archpedi.1972.02110120085007.
2
Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
J Pediatr. 1974 Apr;84(4):534-8. doi: 10.1016/s0022-3476(74)80673-6.
3
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.通过喹吖因荧光鉴定的涉及6号、14号和20号染色体的家族性易位。
Humangenetik. 1971;13(3):205-9. doi: 10.1007/BF00326943.
4
A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.在一名智力发育迟缓的女孩中，通过喹吖因荧光诊断出一条9号环状染色体。
Clin Genet. 1973;4(5):434-41. doi: 10.1111/j.1399-0004.1973.tb01173.x.
5
Pericentric inversion of "fluorescent" segment in chromosome no. 3.3号染色体“荧光”区段的臂间倒位
Humangenetik. 1974;22(4):343-6. doi: 10.1007/BF00295495.
6
Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.通过喹吖因芥子荧光分析鉴定人类中的不同罗伯逊易位
Hereditas. 1971;67(2):213-20. doi: 10.1111/j.1601-5223.1971.tb02375.x.
7
[Identification of several chromosome aberrations in man by the fluorescent method using quinacrine yprite].[利用喹吖因芥子气荧光法鉴定人类的几种染色体畸变]
Tsitologiia. 1976 Feb;18(2):213-8.
8
Immunoglobulin abnormality in a girl with a large chromosome 18.一名患有18号染色体异常增大的女孩的免疫球蛋白异常
J Med Genet. 1972 Sep;9(3):360-5. doi: 10.1136/jmg.9.3.360.
9
Identification of partial 12 trisomy by quinacrine fluorescence.用喹吖因荧光法鉴定部分12三体
J Pediatr. 1973 Feb;82(2):269-72. doi: 10.1016/s0022-3476(73)80165-9.
10
Quinacrine fluorescence for identifying metaphase chromosomes, with special reference to photomicrography.用于鉴定中期染色体的喹吖因荧光法，特别涉及显微摄影术。
Stain Technol. 1972 Mar;47(2):87-93. doi: 10.3109/10520297209116456.

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Fusion genes as biomarkers in pediatric cancers: A review of the current state and applicability in diagnostics and personalized therapy.融合基因作为儿童癌症的生物标志物：当前状况及在诊断和个性化治疗中的适用性综述
Cancer Lett. 2021 Feb 28;499:24-38. doi: 10.1016/j.canlet.2020.11.015. Epub 2020 Nov 25.
2
Pan-Cancer Analysis Reveals the Diverse Landscape of Novel Sense and Antisense Fusion Transcripts.泛癌分析揭示了新型正义和反义融合转录本的多样格局。
Mol Ther Nucleic Acids. 2020 Mar 6;19:1379-1398. doi: 10.1016/j.omtn.2020.01.023. Epub 2020 Jan 29.
3
Balanced translocations in mental retardation.
智力迟钝中的平衡易位
Hum Genet. 2009 Jul;126(1):133-47. doi: 10.1007/s00439-009-0661-6. Epub 2009 Apr 5.
4
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.对新发的明显平衡染色体重排进行荧光原位杂交（FISH）定位，可识别与表型异常相关的特征。
Am J Hum Genet. 2008 Apr;82(4):916-26. doi: 10.1016/j.ajhg.2008.02.007. Epub 2008 Mar 27.
5
Acrocephalopolysyndactyly, pentalogy of Fallot, and hypoacusis in a patient with a de novo reciprocal translocation involving the short arm of chromosome 1 and the long arm of chromosome 18: 46,XX,t(1;18)(p31;q11).一名患有涉及1号染色体短臂和18号染色体长臂的新发相互易位（46,XX,t(1;18)(p31;q11)）的患者出现尖头并指畸形、法洛四联症和听力减退。
J Med Genet. 1993 May;30(5):438-9. doi: 10.1136/jmg.30.5.438.
6
Balanced reciprocal whole arm translocation t(3;9): analysis by fluorescence in situ hybridisation.平衡相互性全臂易位t(3;9)：荧光原位杂交分析
J Med Genet. 1994 Jan;31(1):74-5. doi: 10.1136/jmg.31.1.74.
7
A case of hypogonadism with a translocation: t(4; 12) (q25; q24.2).
Indian J Pediatr. 1994 Jul-Aug;61(4):421-6. doi: 10.1007/BF02751907.
8
A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.一种家族性“平衡”3;9易位，伴有隐匿性8q插入，导致同胞中9p23位点的缺失和重复。
Am J Hum Genet. 1995 Jan;56(1):302-9.
9
High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements.对具有明显平衡结构重排的表型异常患者进行高分辨率染色体分析。
Hum Genet. 1983;63(4):310-4. doi: 10.1007/BF00274751.
10
Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.常染色体的平衡重排：对新生儿调查人群的纵向研究结果
J Med Genet. 1984 Feb;21(1):45-51. doi: 10.1136/jmg.21.1.45.