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. 1973 Dec;6:151–156. doi: 10.1289/ehp.7306151

Uses of banding techniques for the identification of human diseases of cytogenetic origin.

M W Shaw
PMCID: PMC1475549  PMID: 4131094

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Selected References

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

  1. Arrighi F. E., Hsu T. C. Localization of heterochromatin in human chromosomes. Cytogenetics. 1971;10(2):81–86. doi: 10.1159/000130130. [DOI] [PubMed] [Google Scholar]
  2. Caspersson T., Farber S., Foley G. E., Kudynowski J., Modest E. J., Simonsson E., Wagh U., Zech L. Chemical differentiation along metaphase chromosomes. Exp Cell Res. 1968 Jan;49(1):219–222. doi: 10.1016/0014-4827(68)90538-7. [DOI] [PubMed] [Google Scholar]
  3. 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]
  4. Caspersson T., Zech L., Modest E. J., Foley G. E., Wagh U., Simonsson E. Chemical differentiation with fluorescent alkylating agents in Vicia faba metaphase chromosomes. Exp Cell Res. 1969 Nov;58(1):128–140. doi: 10.1016/0014-4827(69)90123-2. [DOI] [PubMed] [Google Scholar]
  5. Chen T. R., Shaw M. W. Stable chromosome changes in human malignant melanoma. Cancer Res. 1973 Sep;33(9):2042–2047. [PubMed] [Google Scholar]
  6. Cohen M. M., Storm D. F., Capraro V. J. A ring chromosome (No. 18) in a cyclops. Clin Genet. 1972;3(4):249–252. doi: 10.1111/j.1399-0004.1972.tb04272.x. [DOI] [PubMed] [Google Scholar]
  7. Comings D. E., Avelino E., Okada T. A., Wyandt H. E. The mechanism of C- and G-banding of chromosomes. Exp Cell Res. 1973 Mar 15;77(1):469–483. doi: 10.1016/0014-4827(73)90601-0. [DOI] [PubMed] [Google Scholar]
  8. Craig-Holmes A. P., Moore F. B., Shaw M. W. Polymorphism of human C-band heterochromatin. I. Frequency of variants. Am J Hum Genet. 1973 Mar;25(2):181–192. [PMC free article] [PubMed] [Google Scholar]
  9. Crandall B. F., Weber F., Muller H. M., Burwell J. K. Identification of 21r and 22r chromosomes by quinacrine fluorescence. Clin Genet. 1972;3(4):264–270. doi: 10.1111/j.1399-0004.1972.tb04275.x. [DOI] [PubMed] [Google Scholar]
  10. De la Chapelle A., Schröder J., Vuopio P. 8-Trisomy in the bone marrow. Report of two cases. Clin Genet. 1972;3(6):470–476. doi: 10.1111/j.1399-0004.1972.tb01483.x. [DOI] [PubMed] [Google Scholar]
  11. Distèche C., Hagemeijer A., Frederic J., Progneaux D. An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry. Clin Genet. 1972;3(5):388–395. doi: 10.1111/j.1399-0004.1972.tb01472.x. [DOI] [PubMed] [Google Scholar]
  12. Drets M. E., Shaw M. W. Specific banding patterns of human chromosomes. Proc Natl Acad Sci U S A. 1971 Sep;68(9):2073–2077. doi: 10.1073/pnas.68.9.2073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dutrillaux B., Lejeune J. Sur une nouvelle technique d'analyse du caryotype humain. C R Acad Sci Hebd Seances Acad Sci D. 1971 May 17;272(20):2638–2640. [PubMed] [Google Scholar]
  14. Dutrillaux B., de Grouchy J., Finaz C., Lejeune J. Mise en évidence de la structure fine des chromosomes humains par digestion enzymatique (pronase en particulier. C R Acad Sci Hebd Seances Acad Sci D. 1971 Aug 2;273(5):587–588. [PubMed] [Google Scholar]
  15. Evans H. J., Buckton K. E., Sumner A. T. Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques. Chromosoma. 1971;35(3):310–325. doi: 10.1007/BF00326281. [DOI] [PubMed] [Google Scholar]
  16. Francke U. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations. Am J Hum Genet. 1972 Mar;24(2):189–213. [PMC free article] [PubMed] [Google Scholar]
  17. George K. P., Polani P. E. Y heterochromatin and XX males. Nature. 1970 Dec 19;228(5277):1215–1216. doi: 10.1038/2281215b0. [DOI] [PubMed] [Google Scholar]
  18. Grace H. J., Ally F. E., Paruk M. A. 46,Xinv(Yp+q-) in four generations of an Indian family. J Med Genet. 1972 Sep;9(3):293–297. doi: 10.1136/jmg.9.3.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Jones K. W. Chromosomal and nuclear location of mouse satellite DNA in individual cells. Nature. 1970 Mar 7;225(5236):912–915. doi: 10.1038/225912a0. [DOI] [PubMed] [Google Scholar]
  20. Jones K. W., Corneo G. Location of satellite and homogeneous DNA sequences on human chromosomes. Nat New Biol. 1971 Oct 27;233(43):268–271. doi: 10.1038/newbio233268a0. [DOI] [PubMed] [Google Scholar]
  21. Jones K. W., Corneo G. Location of satellite and homogeneous DNA sequences on human chromosomes. Nat New Biol. 1971 Oct 27;233(43):268–271. doi: 10.1038/newbio233268a0. [DOI] [PubMed] [Google Scholar]
  22. Jones K. W., Robertson F. W. Localisation of reiterated nucleotide sequences in Drosophila and mouse by in situ hybridisation of complementary RNA. Chromosoma. 1970;31(3):331–345. doi: 10.1007/BF00321229. [DOI] [PubMed] [Google Scholar]
  23. Krmpotic E., Szego K., Modestas R., Molabola G. B. Localization of male determining factor on short arm of Y chromosome. Case report of a baby with 46, x, t (Yp+;14q-). Clin Genet. 1972;3(5):381–387. doi: 10.1111/j.1399-0004.1972.tb01471.x. [DOI] [PubMed] [Google Scholar]
  24. Miller O. J., Miller D. A., Allderdice P. W., Dev V. G., Grewal M. S. Quinacrine fluorescent karyotypes of human diploid and heteroploid cell lines. Cytogenetics. 1971;10(5):338–346. doi: 10.1159/000130152. [DOI] [PubMed] [Google Scholar]
  25. 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]
  26. Pardue M. L., Gall J. G. Chromosomal localization of mouse satellite DNA. Science. 1970 Jun 12;168(3937):1356–1358. doi: 10.1126/science.168.3937.1356. [DOI] [PubMed] [Google Scholar]
  27. Pardue M. L., Gall J. G. Chromosomal localization of mouse satellite DNA. Science. 1970 Jun 12;168(3937):1356–1358. doi: 10.1126/science.168.3937.1356. [DOI] [PubMed] [Google Scholar]
  28. Rowley J. D. Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining. Nature. 1973 Jun 1;243(5405):290–293. doi: 10.1038/243290a0. [DOI] [PubMed] [Google Scholar]
  29. Schnedl W. Analysis of the human karyotype using a reassociation technique. Chromosoma. 1971;34(4):448–454. doi: 10.1007/BF00326316. [DOI] [PubMed] [Google Scholar]
  30. Seabright M. A rapid banding technique for human chromosomes. Lancet. 1971 Oct 30;2(7731):971–972. doi: 10.1016/s0140-6736(71)90287-x. [DOI] [PubMed] [Google Scholar]
  31. Shaw M. W. Human chromosome abnormalities revisited. Am J Hum Genet. 1972 Mar;24(2):227–228. [PMC free article] [PubMed] [Google Scholar]
  32. Sumner A. T., Evans H. J., Buckland R. A. New technique for distinguishing between human chromosomes. Nat New Biol. 1971 Jul 7;232(27):31–32. doi: 10.1038/newbio232031a0. [DOI] [PubMed] [Google Scholar]
  33. Wilson M. G., Towner J. W., Fujimoto A. Retinoblastoma and D-chromosome deletions. Am J Hum Genet. 1973 Jan;25(1):57–61. [PMC free article] [PubMed] [Google Scholar]

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