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Translational Oncology|September 2, 2018
Somatic TP53 Mutations Are Detectable in Circulating Tumor DNA from Children with Anaplastic Wilms TumorsTaryn D Treger, Tasnim Chagtai, Robert Butcher, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 25, 2010
Subtype-specific FBXW7 mutation and MYCN copy number gain in Wilms' tumorRichard D Williams, Reem Al-Saadi, Tasnim Chagtai, et al.
European Journal of Cancer (Oxford, England : 1990)|February 24, 2009
Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1-3 clinical trials: a Children's Cancer and Leukaemia Group (CCLG) StudyBoo Messahel, Richard Williams, Antonia Ridolfi, et al.
Pediatric Nephrology (Berlin, Germany)|October 5, 2021
Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variantMaria Pia Falcone, Kathryn Pritchard-Jones, Jesper Brok, et al.
Nature Communications|January 23, 2015
Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumoursKevin Litchfield, Brenda Summersgill, Shawn Yost, et al.
Journal of Pediatric Surgery|September 27, 2021
Surgical management, staging, and outcomes of Wilms tumours with intravascular extension: Results of the IMPORT studyKristina Dzhuma, Mark Powis, Gordan Vujanic, et al.
Pediatric Blood & Cancer|February 3, 2025
The Clinical Impact of Somatic Copy Number Variations in Patients With Stage IV Wilms Tumor Enrolled in the SIOP 2001 Trial and StudyNils Welter, Reem Al-Saadi, Robinson Gravier-Dumonceau, et al.
Pediatric Blood & Cancer|August 9, 2024
Multimodality detection of tumour rupture in children with Wilms tumourKristina Dzhuma, Minou Oostveen, Tom Watson, et al.
Genes, Chromosomes & Cancer|September 2, 2011
Molecular profiling reveals frequent gain of MYCN and anaplasia-specific loss of 4q and 14q in Wilms tumorRichard D Williams, Reem Al-Saadi, Rachael Natrajan, et al.
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