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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 5, 2017
Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in ChildhoodJonathan D Wasserman, Gail E Tomlinson, Harriet Druker, et al.American Journal of Medical Genetics. Part A|March 28, 2013
Bilateral pheochromocytomas, hemihyperplasia, and subtle somatic mosaicism: the importance of detecting low-level uniparental disomyJennifer M Kalish, Laura K Conlin, Sogol Mostoufi-Moab, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 5, 2017
Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and HepatoblastomaJennifer M Kalish, Leslie Doros, Lee J Helman, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 27, 2024
Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working GroupSuzanne P MacFarland, Kerri Becktell, Kami Wolfe Schneider, et al.Journal of the National Cancer Institute|May 3, 2024
Identification of TP53 germline variants in pediatric patients undergoing tumor testing: strategy and prevalenceMinjie Luo, Derek Wong, Kristin Zelley, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 23, 2025
Update on Tumor Surveillance for Children with Hereditary Pheochromocytoma/Paraganglioma SyndromesSurya P Rednam, Junne Kamihara, Kerri D Becktell, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 15, 2025
Update on Surveillance in Von Hippel-Lindau DiseaseSurya P Rednam, Kerri D Becktell, Anita Villani, et al.Cancer|September 17, 2014
Parent decision-making around the genetic testing of children for germline TP53 mutationsMelissa A Alderfer, Kristin Zelley, Robert B Lindell, et al.The Journal of Molecular Diagnostics : JMD|December 16, 2023
Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-Designed Next-Generation Sequencing PanelFumin Lin, Kajia Cao, Fengqi Chang, et al.Cold Spring Harbor Molecular Case Studies|March 2, 2022
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndromeFeng Xu, Erfan Aref-Eshghi, Jinhua Wu, et al.Pageof 5