Trisomy 21 with XYY
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF02726018.pdf
Reference11 articles.
1. XYY syndrome. In Jones KL, ed.Smith’s Recognisable Patterns of Human Malformation. 5th edn. Philadelphia: WB Saunders Co; 1997. p. 70–71.
2. Ford CE, Jones KW, Mittowich U, Penrose LS, Ridler M, Shapiro A. The chromosome in a patient showing both mangolism and the Klinfelter’s syndrome.Lancet 1959; 1: 709–710.
3. Neu RL, Scheuer AQ, Gardner LI. A case of 48 x 44 +21 in an infant with Down’s syndrome.J Med Genet 1971; 8: 533–535.
4. Hsu LY. Phenotype karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.Am J Med Genet 1994; 53; 108–140.
5. Pettenati MJ, Wheeler M, Bartlett DJ, Subrt I, Rao N, Kroovand RLet al. 45 X/47XYY mosaicism: clinical discrepancy between prenatally and postnatally diagnosed cases.Am J Med Genet 1991; 39 : 42–47.
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