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Volumn , Issue , 2009, Pages 230-236

Preimplantation genetic diagnosis for sex-linked diseases and sex selection for non-medical reasons

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EID: 84891514690     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1017/CBO9780511581571.015     Document Type: Chapter
Times cited : (3)

References (14)
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  • 2
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  • 3
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    • Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia a, x-linked adrenoleukodystrophy, x-linked hydrocephalus and incontinentia pigmenti loci on xq28
    • Gigarel N, Frydman N, Burlet P et al. Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28. Human Genetics2004;114:298–305.
    • (2004) Human Genetics , vol.114 , pp. 298-305
    • Gigarel, N.1    Frydman, N.2    Burlet, P.3
  • 4
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    • Eshre pgd consortium data collection viii: Cycles from january to december 2005 with pregnancy follow-up to october 2006
    • Goossens V, Harton G, Moutou C et al. ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006. Human Reproduction2008;23:2629–45.
    • (2008) Human Reproduction , vol.23 , pp. 2629-2645
    • Goossens, V.1    Harton, G.2    Moutou, C.3
  • 5
    • 0028061446 scopus 로고
    • Clinical experience with preimplantation genetic diagnosis of sex by dual fl uorescent in situ hybridization. Journal of
    • Griffi n DK, Handyside AH, Harper JC et al.Clinical experience with preimplantation genetic diagnosis of sex by dual fl uorescent in situ hybridization. Journal ofAssisted Reproduction and Genetics1994;11:132–43.
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    • Griffi N, D.K.1    Handyside, A.H.2    Harper, J.C.3
  • 6
    • 0025307919 scopus 로고
    • Pregnancies from biopsied human preimplantation embryos sexed by y-specifi c dna amplification
    • Handyside AH, Kontogianni EH, Hardy K and Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specifi c DNA amplification. Nature 1990;344:768–70.
    • (1990) Nature , vol.344 , pp. 768-770
    • Handyside, A.H.1    Kontogianni, E.H.2    Hardy, K.3    Winston, R.M.4
  • 7
    • 0026608740 scopus 로고
    • Biopsy of cleavage stage human embryos and diagnosis of single gene defects by dna amplification
    • Hardy K and Handyside AH. Biopsy of cleavage stage human embryos and diagnosis of single gene defects by DNA amplification. Archives of Pathology andLaboratory Medicine1992;116:388–92.
    • (1992) Archives of Pathology And , vol.116 , pp. 388-392
    • Hardy, K.1    Handyside, A.H.2
  • 8
    • 33744719087 scopus 로고    scopus 로고
    • Pgd for dystrophin gene deletions using fluorescence in situ hybridization
    • Malmgren H, White I, Johansson S et al. PGD for dystrophin gene deletions using fluorescence in situ hybridization. Molecular Human Reproduction2006;12:353–6.
    • (2006) Molecular Human Reproduction , vol.12 , pp. 353-356
    • Malmgren, H.1    White, I.2    Johansson, S.3
  • 9
    • 0028006116 scopus 로고
    • Sex determination of human embryos using the polymerase chain reaction and confirmation by fluorescence in situ hybridization
    • Munne S, Tang YX, Grifo J, Rosenwaks Z and Cohen J. Sex determination of human embryos using the polymerase chain reaction and confirmation by fluorescence in situ hybridization. Fertility and Sterility1994;61:111–17.
    • (1994) Fertility and Sterility , vol.61 , pp. 111-117
    • Munne, S.1    Tang, Y.X.2    Grifo, J.3    Rosenwaks, Z.4    Cohen, J.5
  • 10
    • 84927107653 scopus 로고    scopus 로고
    • McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD), and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD) (September 14, 2007). Available online at
    • Online Mendelian Inheritance in Man (OMIM)tm, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD), and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD) (September 14, 2007). (Available online at: www.ncbi.nlm.nih.gov/omim).
  • 11
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    • Proof of principle and first cases using preimplantation genetic haplotyping – a paradigm shift for embryo diagnosis
    • Renwick PJ, Trussler J, Ostad-Saffari E et al. Proof of principle and first cases using preimplantation genetic haplotyping – a paradigm shift for embryo diagnosis. Reproductive Biomedicine Online2006;13:110–19.
    • (2006) Reproductive Biomedicine Online , vol.13 , pp. 110-119
    • Renwick, P.J.1    Trussler, J.2    Ostad-Saffari, E.3
  • 12
    • 33846481340 scopus 로고    scopus 로고
    • Eshre pgd consortium data collection iv: Cycles from january to december 2003 with pregnancy follow-up to october 2004
    • Sermon KD, Michiels A, Harton G et al.ESHRE PGD Consortium data collection IV: cycles from January to December 2003 with pregnancy follow-up to October 2004. Human Reproduction2007;22:323–6.
    • (2007) Human Reproduction , vol.22 , pp. 323-326
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  • 13
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    • Thornhill AR, de Die-Smulders CE, Geraedts JP et al. ESHRE PGD Consortium “Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)”. HumanReproduction2005;20:35–48.
    • (2005) Reproduction , vol.20 , pp. 35-48
    • Thornhill, A.R.1    De Die-Smulders, C.E.2    Geraedts, J.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.