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Nucleic Acids Research|July 19, 2014
Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancerAlberto L'Abbate, Gemma Macchia, Pietro D'Addabbo, et al.Science (New York, N.Y.)|January 2, 2025
Rare germline structural variants increase risk for pediatric solid tumorsRiaz Gillani, Ryan L Collins, Jett Crowdis, et al.Nature|June 6, 2020
Complement genes contribute sex-biased vulnerability in diverse disordersNolan Kamitaki, Aswin Sekar, Robert E Handsaker, et al.Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.Cell|June 19, 2018
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome SequencingSrinivas R Viswanathan, Gavin Ha, Andreas M Hoff, et al.American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.Nature|May 29, 2020
A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.Nature|September 12, 2014
Gibbon genome and the fast karyotype evolution of small apesLucia Carbone, R Alan Harris, Sante Gnerre, et al.Pageof 2