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DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

Year 2011, Volume: 8 Issue: 4, 338 - 341, 01.12.2011

Resit Koken Aysegül Bukulmez Gulengul Koken Betul Eser Hale Samlı Tevhide Demır Mustafa Solak

Abstract

Keywords

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References

  • Jones KL. XYY Syndrome. Smith’s Recognizable Patterns of Human Malformation 5 th ed. Philadelphia: WB Saunders 1997:70-71.
  • Ford CE, Jones KW, Miller OJ, et al. The chromosomes in a patient showing both mongolism and the Klinefelter syndrome. Lancet 1959;1:709-10.
  • Kovaleva NV, Mutton DE. Epidemiology of double aneu- ploidies involving chromosome 21 and the sex chromo- somes. Am J Med Genet A 2005;134:24-32.
  • Li QY, Tsukishiro S, Nakagawa C, et al. Parental origin and cell stage of non-disjunction of double trisomy in spon- taneous abortion. Congenit Anom (Kyoto) 2005;45:21-5.
  • Al-Aish MS, Dodson WE, Plato CC. Down's syndrome with XYY: 48,XYY, G+. Am J Dis Child 1971;121:444-6.
  • McLean SD. Congenital Anomalies. In: Mhairi G. MacDonald MDM, Mary M.K. Seshia, ed. Avery’s Neonatology Pathophysiology& Management of the Newborn. 6 th ed. Philadelphia: Lippincott Williams& Wilkins, 2005:893- 913.
  • Parmar RC, Muranjan MN, Swami S. Trisomy 21 with XYY. Indian J Pediatr 2002;69:979-81.
  • Widness JA, Pueschel SM, Pezzullo JC, Clemons GK. Elevated erythropoietin levels in cord blood of newborns with Down's syndrome. Biol Neonate 1994;66:50-5.
  • Gollop TR, Naccache NF, Auler-Bittencourt E, et al. Prenatal diagnosis of 48,XYY, +21 ascertained through ul- trasound anomalies. Am J Med Genet 1991;39:76-7.

DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

Year 2011, Volume: 8 Issue: 4, 338 - 341, 01.12.2011

Resit Koken Aysegül Bukulmez Gulengul Koken Betul Eser Hale Samlı Tevhide Demır Mustafa Solak

Abstract

-

Keywords

-

References

  • Jones KL. XYY Syndrome. Smith’s Recognizable Patterns of Human Malformation 5 th ed. Philadelphia: WB Saunders 1997:70-71.
  • Ford CE, Jones KW, Miller OJ, et al. The chromosomes in a patient showing both mongolism and the Klinefelter syndrome. Lancet 1959;1:709-10.
  • Kovaleva NV, Mutton DE. Epidemiology of double aneu- ploidies involving chromosome 21 and the sex chromo- somes. Am J Med Genet A 2005;134:24-32.
  • Li QY, Tsukishiro S, Nakagawa C, et al. Parental origin and cell stage of non-disjunction of double trisomy in spon- taneous abortion. Congenit Anom (Kyoto) 2005;45:21-5.
  • Al-Aish MS, Dodson WE, Plato CC. Down's syndrome with XYY: 48,XYY, G+. Am J Dis Child 1971;121:444-6.
  • McLean SD. Congenital Anomalies. In: Mhairi G. MacDonald MDM, Mary M.K. Seshia, ed. Avery’s Neonatology Pathophysiology& Management of the Newborn. 6 th ed. Philadelphia: Lippincott Williams& Wilkins, 2005:893- 913.
  • Parmar RC, Muranjan MN, Swami S. Trisomy 21 with XYY. Indian J Pediatr 2002;69:979-81.
  • Widness JA, Pueschel SM, Pezzullo JC, Clemons GK. Elevated erythropoietin levels in cord blood of newborns with Down's syndrome. Biol Neonate 1994;66:50-5.
  • Gollop TR, Naccache NF, Auler-Bittencourt E, et al. Prenatal diagnosis of 48,XYY, +21 ascertained through ul- trasound anomalies. Am J Med Genet 1991;39:76-7.
There are 9 citations in total.

Details

Primary Language English
Authors

Resit Koken This is me

Aysegül Bukulmez This is me

Gulengul Koken This is me

Betul Eser This is me

Hale Samlı This is me

Tevhide Demır This is me

Mustafa Solak This is me

Publication Date December 1, 2011
Published in Issue Year 2011 Volume: 8 Issue: 4

Cite

APA Koken, R., Bukulmez, A., Koken, G., … Eser, B. (2011). DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY. European Journal of General Medicine, 8(4), 338-341.
AMA Koken R, Bukulmez A, Koken G, et al. DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY. European Journal of General Medicine. December 2011;8(4):338-341.
Chicago Koken, Resit, Aysegül Bukulmez, Gulengul Koken, Betul Eser, Hale Samlı, Tevhide Demır, and Mustafa Solak. “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”. European Journal of General Medicine 8, no. 4 (December 2011): 338-41.
EndNote Koken R, Bukulmez A, Koken G, Eser B, Samlı H, Demır T, Solak M (December 1, 2011) DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY. European Journal of General Medicine 8 4 338–341.
IEEE R. Koken, A. Bukulmez, G. Koken, B. Eser, H. Samlı, T. Demır, and M. Solak, “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”, European Journal of General Medicine, vol. 8, no. 4, pp. 338–341, 2011.
ISNAD Koken, Resit et al. “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”. European Journal of General Medicine 8/4 (December2011), 338-341.
JAMA Koken R, Bukulmez A, Koken G, Eser B, Samlı H, Demır T, Solak M. DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY. European Journal of General Medicine. 2011;8:338–341.
MLA Koken, Resit et al. “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”. European Journal of General Medicine, vol. 8, no. 4, 2011, pp. 338-41.
Vancouver Koken R, Bukulmez A, Koken G, Eser B, Samlı H, Demır T, et al. DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY. European Journal of General Medicine. 2011;8(4):338-41.