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Proceedings of the National Academy of Sciences of the United States of America|April 10, 2013
Developmental timing of mutations revealed by whole-genome sequencing of twins with acute lymphoblastic leukemiaYussanne Ma, Sara E Dobbins, Amy L Sherborne, et al.
Nature Communications|June 23, 2016
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancerDaniel Chubb, Peter Broderick, Sara E Dobbins, et al.
Environmental Health : a Global Access Science Source|May 4, 2018
Genomic characterization of chronic lymphocytic leukemia (CLL) in radiation-exposed Chornobyl cleanup workersJuhi Ojha, Iryna Dyagil, Stuart C Finch, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 30, 2016
Somatic and Germline TP53 Alterations in Second Malignant Neoplasms from Pediatric Cancer SurvivorsAmy L Sherborne, Vincent Lavergne, Katharine Yu, et al.
Blood|October 31, 2018
Subclonal TP53 copy number is associated with prognosis in multiple myelomaVallari Shah, David C Johnson, Amy L Sherborne, et al.
Blood|September 3, 2013
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotypeGabriele Migliorini, Bettina Fiege, Fay J Hosking, et al.
Nature Genetics|May 11, 2010
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia riskAmy L Sherborne, Fay J Hosking, Rashmi B Prasad, et al.
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