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BMC Genomics|February 1, 2014
Finding the missing honey bee genes: lessons learned from a genome upgradeChristine G Elsik, Kim C Worley, Anna K Bennett, et al.Genome Research|April 10, 2014
Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel linesWen Huang, Andreas Massouras, Yutaka Inoue, et al.Nature Genetics|January 25, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumErica E Davis, Qi Zhang, Qin Liu, et al.American Journal of Human Genetics|January 26, 2016
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 MutationsSeema R Lalani, Pengfei Liu, Jill A Rosenfeld, et al.Nature|February 19, 2010
Complete Khoisan and Bantu genomes from southern AfricaStephan C Schuster, Webb Miller, Aakrosh Ratan, et al.Nature|February 10, 2012
The Drosophila melanogaster Genetic Reference PanelTrudy F C Mackay, Stephen Richards, Eric A Stone, et al.Science (New York, N.Y.)|February 21, 2012
A systematic survey of loss-of-function variants in human protein-coding genesDaniel G MacArthur, Suganthi Balasubramanian, Adam Frankish, et al.JAMA Pediatrics|October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical ManagementLinyan Meng, Mohan Pammi, Anirudh Saronwala, et al.Human Molecular Genetics|November 29, 2022
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney diseaseYang Pan, Xiao Sun, Xuenan Mi, et al.Genome Research|January 6, 2005
Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolutionStephen Richards, Yue Liu, Brian R Bettencourt, et al.Pageof 117