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Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|February 23, 2018
Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case ReportJana Volejnikova, Jirina Zapletalova, Marie Jarosova, et al.
Nature Methods|November 29, 2011
Decoding cell lineage from acquired mutations using arbitrary deep sequencingCheryl A Carlson, Arnold Kas, Robert Kirkwood, et al.
BMC Genomics|January 19, 2013
Use of somatic mutations to quantify random contributions to mouse developmentWenyu Zhou, Yunbing Tan, Donovan J Anderson, et al.
Journal of Hematology & Oncology|April 24, 2014
Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literatureJuehua Gao, Ryan D Gentzler, Andrew E Timms, et al.
Journal of Orthopaedic Trauma|October 21, 2016
The Role of Radiographs and Office Visits in the Follow-Up of Healed Intertrochanteric Hip Fractures: An Economic AnalysisHarish Kempegowda, Raveesh Richard, Amrut Borade, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 7, 2007
Chronic immunodeficiency in mice lacking RasGRP1 results in CD4 T cell immune activation and exhaustionJohn J Priatel, Xiaoxi Chen, Lauren A Zenewicz, et al.
Hepatology (Baltimore, Md.)|February 28, 2007
Prevention of hepatocyte allograft rejection in rats by transferring adenoviral early region 3 genes into donor cellsElena V Mashalova, Chandan Guha, Namita Roy-Chowdhury, et al.
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