Результати пошуку - Senthilkumar A. Natesan
- Показ 1 - 3 результатів із 3
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1
Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders за авторством Senthilkumar A. Natesan, Alan H. Handyside, Alan R. Thornhill, Christian S. Ottolini, Karen Sage, Michael C. Summers, M. Konstantinidis, Dagan Wells, Darren K. Griffin
Опубліковано 2014Artigo -
2
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro за авторством 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
Опубліковано 2014Artigo -
3
Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates за авторством 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
Опубліковано 2015Artigo
Інструменти для пошуку:
Пов'язані теми
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