检索结果 - Senthilkumar A. Natesan

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  1. 1
    Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders

    Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders 由 Senthilkumar A. Natesan, Alan H. Handyside, Alan R. Thornhill, Christian S. Ottolini, Karen Sage, Michael C. Summers, M. Konstantinidis, Dagan Wells, Darren K. Griffin

    出版 2014
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  2. 2
    Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

    Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro 由 Senthilkumar A. Natesan, Alex J. Bladon, Serdar Coşkun, Wafa Qubbaj, R. Prates, S. Munné, Edith Coonen, J. Dreesen, Servi J.C. Stevens, Aimée Paulussen, Sharyn Stock‐Myer, L. Wilton, Souraya Jaroudi, Dagan Wells, Anthony P. Brown, Alan H. Handyside

    出版 2014
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  3. 3
    Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates

    Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates 由 Christian S. Ottolini, Louise Newnham, Antonio Capalbo, Senthilkumar A. Natesan, Hrishikesh Joshi, Danilo Cimadomo, Darren K. Griffin, Karen Sage, Michael C. Summers, Alan R. Thornhill, Elizabeth A. Housworth, Alex Herbert, Laura Rienzi, Filippo Maria Ubaldi, Alan H. Handyside, Eva R. Hoffmann

    出版 2015
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