Risultati della ricerca - Senthilkumar A. Natesan
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1
Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders di Senthilkumar A. Natesan, Alan H. Handyside, Alan R. Thornhill, Christian S. Ottolini, Karen Sage, Michael C. Summers, M. Konstantinidis, Dagan Wells, Darren K. Griffin
Pubblicazione 2014Artigo -
2
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro di 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
Pubblicazione 2014Artigo -
3
Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates di 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
Pubblicazione 2015Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Gene
Genetics
Aneuploidy
Chromosome
Embryo
Meiosis
Preimplantation genetic diagnosis
Abnormality
Blastomere
Centromere
Chromatid
Chromosomal crossover
Chromosome segregation
Context (archaeology)
Embryogenesis
Genome
Genotype
Genotyping
Haplotype
Homologous recombination
Human genome
Medicine
Meiosis II
Paleontology
Polar body
Psychiatry
Recombination
Reference genome
Single-nucleotide polymorphism