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Plos One|December 7, 2018
The impact of a fine-scale population stratification on rare variant association test resultsElodie Persyn, Richard Redon, Lise Bellanger, et al.
Human Molecular Genetics|February 26, 2011
FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formationGeorge Koumbaris, Hariklia Hatzisevastou-Loukidou, Angelos Alexandrou, et al.
Bioinformatics (Oxford, England)|October 11, 2011
Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIMEPierre Lindenbaum, Solena Le Scouarnec, Vincent Portero, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Issues in Law & Medicine|May 5, 2021
"You Are Beautiful, No Matter What They Say": Applying An Evidence-Based Approach To Body Image LawMarilyn Bromberg, Madeleine Hay, Tomas Fitzgerald, et al.
Biochemical Society Transactions|March 20, 2010
Confirmed rare copy number variants implicate novel genes in schizophreniaGloria W C Tam, Louie N van de Lagemaat, Richard Redon, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 1, 2004
Chromosome paints from single copies of chromosomesSusan Gribble, Bee L Ng, Elena Prigmore, et al.
Cell|September 2, 2004
Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibersNick Gilbert, Shelagh Boyle, Heike Fiegler, et al.
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