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A case of trisomy for the short arm of chromosome No. 9(+9(p))

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Summary

A new case of “free” trisomy for the short arm of No. 9 chromosome identified by Giemsa staining and “Giemsa-11 technique” is reported.

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References

  1. Baccichetti, C., Tenconi, R.: A new case of trisomy for the short arm of No. 9 chromosome. J. med. Genet. 10, 296–299 (1973)

  2. Bobrow, M., Madan, K., Pearson, P. L.: Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9. Nature (Lond.) New Biol. 238, 122–124 (1972)

  3. Ebbin, A. J., Wilson, M. G., Towner, J. W., Slaughter, J. P.: Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18. J. med. Genet. 10, 65–69 (1973)

  4. Hoehn, H., Engel, W., Reinwein, H.: Presumed trisomy for the short arm of No. 9 chromosome not due to inherited translocation. Humangenetik 12, 175–181 (1971)

  5. Podruch, P. E., Weisskopf, B.: Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15p+;9q-) in three generations. J. Pediat. 85, 92–95 (1974)

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  8. Schmid, W., Vischer, D.: Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome No. 9. Humangenetik 7, 22–27 (1969)

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Käosaar, M.E., Mikelsaar, A.-.N., Talvik, T.A. et al. A case of trisomy for the short arm of chromosome No. 9(+9(p)). Hum Genet 34, 77–80 (1976). https://doi.org/10.1007/BF00284440

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Keywords

  • Internal Medicine
  • Metabolic Disease
  • Giemsa Staining