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Journal Abstract Search

158 related items for PubMed ID: 26484079

  • 21. Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos.
    Colls P, Escudero T, Fischer J, Cekleniak NA, Ben-Ozer S, Meyer B, Damien M, Grifo JA, Hershlag A, Munné S.
    Reprod Biomed Online; 2012 Jun; 24(6):621-9. PubMed ID: 22503275
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  • 24. An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening.
    Chang LJ, Chen SU, Tsai YY, Hung CC, Fang MY, Su YN, Yang YS.
    Clin Exp Reprod Med; 2011 Sep; 38(3):126-34. PubMed ID: 22384431
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  • 25. Polar body analysis by array comparative genomic hybridization accurately predicts aneuploidies of maternal meiotic origin in cleavage stage embryos of women of advanced maternal age.
    Christopikou D, Tsorva E, Economou K, Shelley P, Davies S, Mastrominas M, Handyside AH.
    Hum Reprod; 2013 May; 28(5):1426-34. PubMed ID: 23477909
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  • 26. Evolution of aneuploidy up to Day 4 of human preimplantation development.
    Mertzanidou A, Spits C, Nguyen HT, Van de Velde H, Sermon K.
    Hum Reprod; 2013 Jun; 28(6):1716-24. PubMed ID: 23526301
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  • 30. Number of embryos biopsied as a predictive indicator for the outcome of preimplantation genetic diagnosis by fluorescence in situ hybridisation in translocation cases.
    Tulay P, Gultomruk M, Findikli N, Bahceci M.
    Zygote; 2016 Feb; 24(1):107-14. PubMed ID: 25601127
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  • 36. PGD for a complex chromosomal rearrangement by array comparative genomic hybridization.
    Vanneste E, Melotte C, Voet T, Robberecht C, Debrock S, Pexsters A, Staessen C, Tomassetti C, Legius E, D'Hooghe T, Vermeesch JR.
    Hum Reprod; 2011 Apr; 26(4):941-9. PubMed ID: 21292638
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  • 37. First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.
    Wells D, Escudero T, Levy B, Hirschhorn K, Delhanty JD, Munné S.
    Fertil Steril; 2002 Sep; 78(3):543-9. PubMed ID: 12215331
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  • 38. Multicolor detection of every chromosome as a means of detecting mosaicism and nuclear organization in human embryonic nuclei.
    Turner K, Fowler K, Fonseka G, Griffin D, Ioannou D.
    Panminerva Med; 2016 Jun; 58(2):175-90. PubMed ID: 26982524
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