Risk assessment and prenatal diagnosis in a recent pregnancy in a family with a child with Down syndrome due to t ( 21q;21q )

Risk assessment and prenatal diagnosis in a recent pregnancy in a family with a child with Down syndrome due to t ( 21q;21q )

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  • 1.Thompson & Thompson, Genetics inMedicine. W.B. Saunders Company.Fifth Edition, pp: 219-222, 1991.
  • 2.Maeda T, Ohno M, Nishida H: Clinicaland cytogenetic studies of two infantswith partial monosomy G. Hum. Genet.35: 255-259, 1997.
  • 3.Cantu JM, Hernandez A, PlascenicaML, Vaca G, Moller M and Rivera H:Partial trisomy and monosomy 21 in aninfant with an unusal de novo 21;21translocation. Ann Genet. 23: 183-186, 1980.
  • 4.Sachs ES, Jahoda MG, Los FJ, PijpersL, Wladimiroff JM: Trisomy 21mosaicism in gonads withunexpectedly high recurrence risks.Biochem Cell Biol. 7: 186-188, 1990.,
  • 5.Brock DH, Rodeck CH, Ferguson-Smith MA eds, Prenatal Diagnosis andScreening. Longman Group. UK, FirstEdition, pp: 371-376, 1992.
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Turkish Journal of Medical Sciences-Cover
  • ISSN: 1300-0144
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
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