Canlyniadau Chwilio - 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 gan Senthilkumar A. Natesan, Alan H. Handyside, Alan R. Thornhill, Christian S. Ottolini, Karen Sage, Michael C. Summers, M. Konstantinidis, Dagan Wells, Darren K. Griffin

    Cyhoeddwyd 2014
    Cael y testun llawn Cael y testun llawn
    Artigo
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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 gan 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

    Cyhoeddwyd 2014
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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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 gan 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

    Cyhoeddwyd 2015
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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