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Showing results (281-290 of 285) with videos related to

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Bioinformatics (Oxford, England)|May 9, 2007
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomesE Dicks, J W Teague, P Stephens, et al.
Anaesthesia and Intensive Care|October 6, 2011
Experience with high frequency oscillation ventilation during the 2009 H1N1 influenza pandemic in Australia and New ZealandR J Boots, J Lipman, M Lassig-Smith, et al.
Pediatric Cardiology|November 24, 2022
Pediatric Cardiology Fellowship Standards for Training in Exercise Medicine and Curriculum OutlineJ H Huang, S G Wittekind, A R Opotowsky, et al.
Blood Cancer Journal|February 25, 2017
Bi-allelic inactivation is more prevalent at relapse in multiple myeloma, identifying RB1 as an independent prognostic markerS S Chavan, J He, R Tytarenko, et al.
Nature Communications|June 19, 2021
Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESSA Rose Brannon, Gowtham Jayakumaran, Monica Diosdado, et al.
Pageof 29

Showing results (281-290 of 285) with videos related to

Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 285 results.
Bioinformatics (Oxford, England)|May 9, 2007
AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomesE Dicks, J W Teague, P Stephens, et al.
Anaesthesia and Intensive Care|October 6, 2011
Experience with high frequency oscillation ventilation during the 2009 H1N1 influenza pandemic in Australia and New ZealandR J Boots, J Lipman, M Lassig-Smith, et al.
Pediatric Cardiology|November 24, 2022
Pediatric Cardiology Fellowship Standards for Training in Exercise Medicine and Curriculum OutlineJ H Huang, S G Wittekind, A R Opotowsky, et al.
Blood Cancer Journal|February 25, 2017
Bi-allelic inactivation is more prevalent at relapse in multiple myeloma, identifying RB1 as an independent prognostic markerS S Chavan, J He, R Tytarenko, et al.
Nature Communications|June 19, 2021
Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESSA Rose Brannon, Gowtham Jayakumaran, Monica Diosdado, et al.
Pageof 29