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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 17, 2018
Metastatic Choriocarcinoma Masquerading as a Congenital Glabellar HemangiomaSteve Taylor, Kimberly Eisenstein, Vanessa Gildenstern, et al.Biopreservation and Biobanking|July 14, 2025
Development of a Multimedia Electronic Consent Platform for Biobanking and Research Utilizing Opinions from Children, Teens, and AdultsIryna Kayda, Ashton Ellis, Vi Nguyen, et al.Molecular Cancer|February 27, 2010
A genome-wide screen identifies frequently methylated genes in haematological and epithelial cancersThomas Dunwell, Luke Hesson, Tibor A Rauch, et al.Journal of Child Neurology|October 22, 2013
Detection of an atypical teratoid rhabdoid brain tumor gene deletion in circulating blood using next-generation sequencingMadhavi Chakravadhanula, Waibhav Tembe, Christophe Legendre, et al.Molecular Cancer|July 3, 2009
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemiasLuke B Hesson, Thomas L Dunwell, Wendy N Cooper, et al.Scientific Reports|July 5, 2022
Virtual reality for the observation of oncology models (VROOM): immersive analytics for oncology patient cohortsChng Wei Lau, Zhonglin Qu, Daniel Draper, et al.Epigenetics|May 12, 2009
Epigenetic analysis of childhood acute lymphoblastic leukemiaThomas L Dunwell, Luke B Hesson, Tatiana Pavlova, et al.Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|January 9, 2010
Respiratory viruses, a common microbiological finding in neutropenic children with feverAnna Lindblom, Vivek Bhadri, Stefan Söderhäll, et al.Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.Blood|July 30, 2008
High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survivalDaniel T Starczynowski, Suzanne Vercauteren, Adele Telenius, et al.Pageof 11