Uses of banding techniques for the identification of human diseases of cytogenetic origin.
作者信息
Shaw M W
出版信息
Environ Health Perspect. 1973 Dec;6:151-6. doi: 10.1289/ehp.7306151.
Abstract
摘要
相似文献
1
Uses of banding techniques for the identification of human diseases of cytogenetic origin.染色体显带技术在人类细胞遗传学起源疾病鉴定中的应用。
Environ Health Perspect. 1973 Dec;6:151-6. doi: 10.1289/ehp.7306151.
2
Application of new staining techniques to the study of human chromosomes.新染色技术在人类染色体研究中的应用。
Prog Med Genet. 1973;9:1-47.
3
Genetic abnormalities as biological tumor markers.
Semin Oncol. 1987 Jun;14(2):213-31.
4
Updating advances in cytogenetics. Applications of the new chromosome banding methods.细胞遗传学的最新进展。新染色体显带方法的应用。
Birth Defects Orig Artic Ser. 1974;10(8):7-18.
5
[Stereotyped chromosome abnormalities in human leukemia and lymphoma].[人类白血病和淋巴瘤中的定型染色体异常]
Presse Med. 1983 Dec 17;12(46):2937-41.
6
7
Chromosomal mechanisms in neoplasia.肿瘤形成中的染色体机制。
Prog Clin Biol Res. 1985;177:139-52.
8
Cytogenetics and somatic cell genetics: the impact of chromosome banding.细胞遗传学与体细胞遗传学：染色体显带的影响
Birth Defects Orig Artic Ser. 1977;13(6):79-103.
9
Application of cytogenetics in neoplastic diseases.细胞遗传学在肿瘤性疾病中的应用。
Crit Rev Clin Lab Sci. 1985;22(3):219-74. doi: 10.3109/10408368509165844.
10
Human chromosome analysis.人类染色体分析。
Am Fam Physician. 1975 Apr;11(4):76-89.
引用本文的文献
1
Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors.利用CRISPR碱基编辑器和引导编辑器的mRNA在人诱导多能干细胞中高效产生和纠正突变
Genes (Basel). 2020 May 6;11(5):511. doi: 10.3390/genes11050511.
2
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis.联合实验和系统水平分析揭示了 miR-124 在人类神经发生过程中的复杂调控网络。
Cell Syst. 2018 Oct 24;7(4):438-452.e8. doi: 10.1016/j.cels.2018.08.011. Epub 2018 Oct 3.
本文引用的文献
1
Chemical differentiation along metaphase chromosomes.沿中期染色体的化学分化。
Exp Cell Res. 1968 Jan;49(1):219-22. doi: 10.1016/0014-4827(68)90538-7.
2
Localisation of reiterated nucleotide sequences in Drosophila and mouse by in situ hybridisation of complementary RNA.通过互补RNA原位杂交对果蝇和小鼠中重复核苷酸序列进行定位。
Chromosoma. 1970;31(3):331-45. doi: 10.1007/BF00321229.
3
Y heterochromatin and XX males.
Nature. 1970 Dec 19;228(5277):1215-6. doi: 10.1038/2281215b0.
4
Chromosomal localization of mouse satellite DNA.小鼠卫星DNA的染色体定位
Science. 1970 Jun 12;168(3937):1356-8. doi: 10.1126/science.168.3937.1356.
5
Chromosomal and nuclear location of mouse satellite DNA in individual cells.小鼠卫星DNA在单个细胞中的染色体和核定位。
Nature. 1970 Mar 7;225(5236):912-5. doi: 10.1038/225912a0.
6
Chemical differentiation with fluorescent alkylating agents in Vicia faba metaphase chromosomes.蚕豆中期染色体中荧光烷基化剂的化学分化
Exp Cell Res. 1969 Nov;58(1):128-40. doi: 10.1016/0014-4827(69)90123-2.
7
Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis.
Exp Cell Res. 1970 Nov;63(1):238-40. doi: 10.1016/0014-4827(70)90362-9.
8
Quinacrine fluorescent karyotypes of human diploid and heteroploid cell lines.人类二倍体和异倍体细胞系的喹吖因荧光核型
Cytogenetics. 1971;10(5):338-46. doi: 10.1159/000130152.
9
46,Xinv(Yp+q-) in four generations of an Indian family.一个印度家庭四代人中出现的46,Xinv(Yp+q-)
J Med Genet. 1972 Sep;9(3):293-7. doi: 10.1136/jmg.9.3.293.
10
Identification of 21r and 22r chromosomes by quinacrine fluorescence.通过喹吖因荧光鉴定21号和22号染色体。
Clin Genet. 1972;3(4):264-70. doi: 10.1111/j.1399-0004.1972.tb04275.x.
Zotero 插件