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. 1972 Mar;9(1):1–7. doi: 10.1136/jmg.9.1.1

Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.

T Caspersson, J Lindsten, L Zech, K E Buckton, W H Price
PMCID: PMC1469203  PMID: 4112567

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Selected References

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

  1. Boué J. G., Boué A. Fréquence des aberrations chromosomiques dans les avortements spontanés humains. C R Acad Sci Hebd Seances Acad Sci D. 1969 Jul 16;269(2):283–288. [PubMed] [Google Scholar]
  2. 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]
  3. 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]
  4. De la Chapelle A., Wennström J., Wasastjerna C., Knutar F., Stenman U. H., Weber T. H. Apparent C trisomy in bone marrow cells. Report of two cases. Scand J Haematol. 1970;7(2):112–122. doi: 10.1111/j.1600-0609.1970.tb01877.x. [DOI] [PubMed] [Google Scholar]
  5. Gustavson K. H., Hagberg B., Santesson B. Mosaic trisomy of an autosome in the 6-12 group in a patient with multiple congenital anomalies. Acta Paediatr Scand. 1967 Nov;56(6):681–686. doi: 10.1111/j.1651-2227.1967.tb15996.x. [DOI] [PubMed] [Google Scholar]
  6. Hellström K., Hagenfeldt L., Larsson A., Lindsten J., Sundelin P., Tiepolo L. An extra C chromosome and various metabolic abnormalities in the bone marrow from a patient with refractory sideroblastic anaemia. Scand J Haematol. 1971;8(4):293–306. doi: 10.1111/j.1600-0609.1971.tb00878.x. [DOI] [PubMed] [Google Scholar]
  7. JACOBS P. A., HARNDEN D. G., BUCKTON K. E., BROWN W. M., KING M. J., McBRIDE J. A., MACGREGOR T. N., MACLEAN N. Cytogenetic studies in primary amenorrhoea. Lancet. 1961 Jun 3;1(7188):1183–1189. doi: 10.1016/s0140-6736(61)91939-0. [DOI] [PubMed] [Google Scholar]
  8. Jalbert P., Jobert J., Patet J., Mouriquand C., Roget J. Un nouveau cas de trisomie présumée 6-12. Ann Genet. 1966 Sep;9(3):109–112. [PubMed] [Google Scholar]
  9. Juberg R. C., Gilbert E. F., Salisbury R. S. Trisomy C in an infant with polycystic kidneys and other malformations. J Pediatr. 1970 Apr;76(4):598–603. doi: 10.1016/s0022-3476(70)80411-5. [DOI] [PubMed] [Google Scholar]
  10. PFEIFFER R. A., SCHELLONG G., KOSENOW W. [Chromosome anomalies in the blood cells of a child with multiple abnormalities]. Klin Wochenschr. 1962 Oct 15;40:1058–1067. doi: 10.1007/BF01484591. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. Wolf U., Reinwein H. Chromosomenmosaik C-Trisomie/normal. Humangenetik. 1965;1(7):686–687. [PubMed] [Google Scholar]
  13. de Grouchy J., Turleau C., Léonard C. Etude en fluorescence d'une trisomie C mosaique, probablement 8: 46,XY-47,XY,?8+. Ann Genet. 1971 Mar;14(1):69–72. [PubMed] [Google Scholar]

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