A case of trisomy 8 mosaicism

A case of trisomy 8 mosaicism

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  • 1.Glbert-Barness GF, Opitz JM. Chromo-somal abnormalities. In: WigglesworthJS, Singer DB (eds). Textbook of Fetaland Perinatal Pathology. Boston: Black-well Scientific Publ., 1991, pp: 339-79.
  • 2.Jones KL. Smith’s Recognizable Pat-terns of Human Malformation. Phil-adelphia: WB Saunders Comp., 1988,pp:26-9.
  • 3.Hirschorn K. Clinical abnormalities ofthe autosomes. In: Behrmann RE, Klieg-man RM, Waldo EN, Vaughan VC,(eds). Nelson Textbook of Pediatrics.Philadelpia: WB Saunders Comp.,1992, pp: 286-7.
  • 4.Engelen JJ, de Die-Smulders CE, Sij-stermans JM, Meers LE, Albrechts JS,Hamers AJ. Familial partial trisomy 8pwithout dysmorphic features and onlymild mental retardation. J Med Genet32: 792-5, 1995.
  • 5.Niss R, Passarge E. Trisomy 8 re-stricted to cultured skin fibroblasts. JMed Genet 13: 229, 1976.
Turkish Journal of Medical Sciences-Cover
  • ISSN: 1300-0144
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
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