Loading [a11y]/accessibility-menu.js
 
BibTex RIS Kaynak Göster

DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY

Yıl 2011, Cilt: 8 Sayı: 4, 338 - 341, 01.12.2011

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

Öz

Anahtar Kelimeler

-

Kaynakça

  • 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

Yıl 2011, Cilt: 8 Sayı: 4, 338 - 341, 01.12.2011

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

Öz

-

Anahtar Kelimeler

-

Kaynakça

  • 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.
Toplam 9 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Olgu Sunumu
Yazarlar

Resit Koken Bu kişi benim

Aysegül Bukulmez Bu kişi benim

Gulengul Koken Bu kişi benim

Betul Eser Bu kişi benim

Hale Samlı Bu kişi benim

Tevhide Demır Bu kişi benim

Mustafa Solak Bu kişi benim

Yayımlanma Tarihi 1 Aralık 2011
Yayımlandığı Sayı Yıl 2011 Cilt: 8 Sayı: 4

Kaynak Göster

APA Koken, R., Bukulmez, A., Koken, G., Eser, B., vd. (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, Eser B, Samlı H, Demır T, Solak M. DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY. European Journal of General Medicine. Aralık 2011;8(4):338-341.
Chicago Koken, Resit, Aysegül Bukulmez, Gulengul Koken, Betul Eser, Hale Samlı, Tevhide Demır, ve Mustafa Solak. “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”. European Journal of General Medicine 8, sy. 4 (Aralık 2011): 338-41.
EndNote Koken R, Bukulmez A, Koken G, Eser B, Samlı H, Demır T, Solak M (01 Aralık 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, ve M. Solak, “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”, European Journal of General Medicine, c. 8, sy. 4, ss. 338–341, 2011.
ISNAD Koken, Resit vd. “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”. European Journal of General Medicine 8/4 (Aralık 2011), 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 vd. “DOUBLE ANEUPLOIDY: A CASE OF TRISOMY 21 WITH XYY”. European Journal of General Medicine, c. 8, sy. 4, 2011, ss. 338-41.
Vancouver 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(4):338-41.