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The Journal of Clinical Endocrinology and Metabolism|July 9, 2014
Germline FH mutations presenting with pheochromocytomaGraeme R Clark, Marco Sciacovelli, Edoardo Gaude, et al.Journal of Medical Genetics|January 16, 2021
Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancersD Gareth Evans, Fiona Lalloo, Neil Aj Ryan, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 17, 2008
Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCNEmma R Woodward, Christopher Ricketts, Pip Killick, et al.International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.Genes, Chromosomes & Cancer|January 17, 2020
Characterization of renal cell carcinoma-associated constitutional chromosome abnormalities by genome sequencingPhilip S Smith, James Whitworth, Hannah West, et al.European Urology Oncology|December 14, 2019
Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected IndividualsClaire Forde, Derek H K Lim, Yousef Alwan, et al.Human Mutation|September 4, 2013
UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor geneNaomi C Wake, Christopher J Ricketts, Mark R Morris, et al.Journal of Medical Genetics|September 18, 2017
CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testingJosie Innes, Lisa Reali, Jill Clayton-Smith, et al.Cancers|August 27, 2021
Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 ProbabilityD Gareth Evans, Elke M van Veen, Emma R Woodward, et al.Gut|October 1, 2020
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypesMariona Terradas, Pilar Mur, Sami Belhadj, et al.Pageof 9