Skip to main content

. 1972 Mar;24(2):189–213.

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

PMCID: PMC1762196 PMID: 5016511

212

Images in this article

Fig. 1
on p.196

Fig. 3
on p.198

Fig. 4
on p.199

Fig. 5
on p.200

Fig. 7
on p.203

Fig. 9
on p.205

Fig. 10
on p.206

Fig. 11
on p.208

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Adams G. L., Kivowitz J., Ziskind E. Manic depressive psychosis, mental retardation, and chromosomal rearrangement. Arch Gen Psychiatry. 1970 Oct;23(4):305–309. doi: 10.1001/archpsyc.1970.01750040017003. [DOI] [PubMed] [Google Scholar]
Carrel R. E., Sparkes R. S., Wright S. W. Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies. J Pediatr. 1971 Apr;78(4):664–672. doi: 10.1016/s0022-3476(71)80471-7. [DOI] [PubMed] [Google Scholar]
Caspersson T., Gahrton G., Lindsten J., Zech L. Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis. Exp Cell Res. 1970 Nov;63(1):238–240. doi: 10.1016/0014-4827(70)90362-9. [DOI] [PubMed] [Google Scholar]
Caspersson T., Lindsten J., Zech L. Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence. Exp Cell Res. 1970 Aug;61(2):475–476. doi: 10.1016/0014-4827(70)90479-9. [DOI] [PubMed] [Google Scholar]
Caspersson T., Lomakka G., Zech L. The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability. Hereditas. 1972;67(1):89–102. doi: 10.1111/j.1601-5223.1971.tb02363.x. [DOI] [PubMed] [Google Scholar]
Caspersson T., Zech L., Johansson C. Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents. Exp Cell Res. 1970 Oct;62(2):490–492. doi: 10.1016/0014-4827(70)90586-0. [DOI] [PubMed] [Google Scholar]
Caspersson T., Zech L., Johansson C., Modest E. J. Identification of human chromosomes by DNA-binding fluorescent agents. Chromosoma. 1970;30(2):215–227. doi: 10.1007/BF00282002. [DOI] [PubMed] [Google Scholar]
Caspersson T., Zech L., Modest E. J. Fluorescent labeling of chromosomal DNA: superiority of quinacrine mustard to quinacrine. Science. 1970 Nov 13;170(3959):762–762. doi: 10.1126/science.170.3959.762. [DOI] [PubMed] [Google Scholar]
Caspersson T., Zech L., Modest E. J., Foley G. E., Wagh U., Simonsson E. DNA-binding fluorochromes for the study of the organization of the metaphase nucleus. Exp Cell Res. 1969 Nov;58(1):141–152. doi: 10.1016/0014-4827(69)90124-4. [DOI] [PubMed] [Google Scholar]
Craig A. P., Shaw M. W. Autoradiographic studies of the human Y chromosome. Chromosoma. 1971 Mar 16;32(4):364–377. doi: 10.1007/BF00285250. [DOI] [PubMed] [Google Scholar]
Crandall B. F., Carrel R. E., Adams G. L., Sparkes R. S. Cytogenetic studies in a patient with a de novo t(Cq-;Gp+). J Med Genet. 1970 Dec;7(4):413–416. doi: 10.1136/jmg.7.4.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
George K. P. Cytochemical differentiation along human chromosomes. Nature. 1970 Apr 4;226(5240):80–81. doi: 10.1038/226080a0. [DOI] [PubMed] [Google Scholar]
Gripenberg U. Chromosome studies in some virus infections. Hereditas. 1965;54(1):1–18. doi: 10.1111/j.1601-5223.1965.tb02003.x. [DOI] [PubMed] [Google Scholar]
LEWIS E. B. The phenomenon of position effect. Adv Genet. 1950;3:73–115. doi: 10.1016/s0065-2660(08)60083-8. [DOI] [PubMed] [Google Scholar]
Miller D. A., Allderdice P. W., Miller O. J., Breg W. R. Quinacrine fluorescence patterns of human D group chromosomes. Nature. 1971 Jul 2;232(5305):24–27. doi: 10.1038/232024a0. [DOI] [PubMed] [Google Scholar]
O'Riordan M. L., Robinson J. A., Buckton K. E., Evans H. J. Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence. Nature. 1971 Mar 19;230(5290):167–168. doi: 10.1038/230167a0. [DOI] [PubMed] [Google Scholar]
Pearson P. L., Bobrow M., Vosa C. G. Technique for identifying Y chromosomes in human interphase nuclei. Nature. 1970 Apr 4;226(5240):78–80. doi: 10.1038/226078a0. [DOI] [PubMed] [Google Scholar]
Rethoré M. O., Larget-Piet L., Abonyi D., Boeswillwald M., Berger R., Carpentier S., Cruveiller J., Dutrillau B., Lafourcade J., Penneau M. Sur quatre cas de trisomie pour le bras court du chromosome 9. Individualisation d'une nouvelle entite morbide. Ann Genet. 1970 Dec;13(4):217–232. [PubMed] [Google Scholar]
SCHMID W. DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES. Cytogenetics. 1963;2:175–193. doi: 10.1159/000129778. [DOI] [PubMed] [Google Scholar]
Sumner A. T., Robinson J. A., Evans H. J. Distingiishing between X, Y and YY-bearing human spermatozoa by fluorescence and DNA content. Nat New Biol. 1971 Feb 24;229(8):231–233. doi: 10.1038/newbio229231a0. [DOI] [PubMed] [Google Scholar]
UHL C. H. CHROMOSOME STRUCTURE AND CROSSING OVER. Genetics. 1965 Feb;51:191–207. doi: 10.1093/genetics/51.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

PDF (4.5 MB)

RESOURCES