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Reciprocal chromosome translocations: analysis of two mutants by interactive computer.

作者信息

Dickerson R W, Xuong N H, Jones O W

出版信息

J Med Genet. 1972 Dec;9(4):422-9. doi: 10.1136/jmg.9.4.422.

DOI:10.1136/jmg.9.4.422
PMID:4646549
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1469061/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/58341394a457/jmedgene00363-0045-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/2a0bbd478fe5/jmedgene00363-0042-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/1136b27c2127/jmedgene00363-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/58341394a457/jmedgene00363-0045-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/2a0bbd478fe5/jmedgene00363-0042-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/1136b27c2127/jmedgene00363-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7722/1469061/58341394a457/jmedgene00363-0045-a.jpg

相似文献

1
Reciprocal chromosome translocations: analysis of two mutants by interactive computer.相互染色体易位:通过交互式计算机对两个突变体进行分析。
J Med Genet. 1972 Dec;9(4):422-9. doi: 10.1136/jmg.9.4.422.
2
Noninvolvement of the human X chromosome in X-ray induced exchanges.人类X染色体未参与X射线诱导的交换。
Cytogenet Cell Genet. 1973;12(5):342-56. doi: 10.1159/000130473.
3
Nonrandom distribution of chromosome breaks in Fanconi's anemia.范科尼贫血中染色体断裂的非随机分布。
Cytogenet Cell Genet. 1973;12(6):423-34. doi: 10.1159/000130485.
4
Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.范科尼贫血:1例骨髓细胞存在显著染色体异常患者的报告。
J Med Genet. 1972 Dec;9(4):474-8. doi: 10.1136/jmg.9.4.474.
5
[A comparative study of the frequency of stable and unstable chromosome aberrations in the gamma irradiation of human lymphocytes in vitro].[体外γ射线照射人淋巴细胞时稳定和不稳定染色体畸变频率的比较研究]
Radiats Biol Radioecol. 1995 Sep-Oct;35(5):611-8.
6
Chromosome studies in a neonatal population.新生儿群体的染色体研究。
Can Med Assoc J. 1972 Apr 8;106(7):776-9.
7
[The most frequent chromosomal abnormalities in karyotypes of patients with reproductive problems].[生殖问题患者核型中最常见的染色体异常情况]
Tsitol Genet. 2007 Jul-Aug;41(4):48-55.
8
Computer-assisted karyotyping.
J Reprod Med. 1976 Jul;17(1):53-7.
9
Application of new technics of chromosome identification to cytogenetic problems.
Birth Defects Orig Artic Ser. 1973 Jan;9(1):171-82.
10
Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case.在一例复查病例中,通过微密度测定法鉴定2号染色体的臂间倒位和7号染色体短臂的重复。
Hum Hered. 1973 Apr;23(4):331-7. doi: 10.1159/000152593.

本文引用的文献

1
HIGH-SPEED AUTOMATIC ANALYSIS OF BIOMEDICAL PICTURES.生物医学图像的高速自动分析
Science. 1964 Oct 9;146(3641):216-23.
2
Computer-oriented analysis of human chromosomes. I. Photometric estimation of DNA content.人类染色体的计算机辅助分析。I. DNA含量的光度测定
Cytogenetics. 1966;5(3):223-42. doi: 10.1159/000129899.
3
Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl.从小量全血接种物培养白细胞,并通过用低渗氯化钾处理制备中期染色体。
Stain Technol. 1965 Nov;40(6):333-8. doi: 10.3109/10520296509116440.
4
An interactive computer program for chromosome analysis.
Comput Biomed Res. 1969 Feb;2(3):274-90. doi: 10.1016/0010-4809(69)90006-8.
5
A problem of pattern recognition in the automatic analysis of chromosomes: locating the centromere.染色体自动分析中的模式识别问题:着丝粒定位
Comput Biomed Res. 1968 Oct;2(2):187-97. doi: 10.1016/0010-4809(68)90037-2.
6
Improved computer chromosome analysis incorporating preprocessing and boundary analysis.
Phys Med Biol. 1970 Jul;15(3):435-45. doi: 10.1088/0031-9155/15/3/004.
7
Chromosomal abnormalities in the human population: estimation of rates based on New Haven newborn study.人类群体中的染色体异常:基于纽黑文新生儿研究的发生率估计
Science. 1970 Jul 31;169(3944):495-7. doi: 10.1126/science.169.3944.495.
8
Differential binding of alkylating fluorochromes in human chromosomes.烷化荧光染料在人类染色体中的差异结合
Exp Cell Res. 1970 Jun;60(3):315-9. doi: 10.1016/0014-4827(70)90523-9.
9
Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.人染色体的喹吖因氮芥荧光:异常易位的特征
Am J Hum Genet. 1972 Mar;24(2):189-213.
10
The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability.人类中期染色体的24种荧光模式——鉴别特征与变异性
Hereditas. 1972;67(1):89-102. doi: 10.1111/j.1601-5223.1971.tb02363.x.