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Seminars in Oncology|September 29, 2018
Rapid disease progression in a patient with mismatch repair-deficient and cortisol secreting adrenocortical carcinoma treated with pembrolizumabR T Casey, O Giger, I Seetho, et al.
Oncogene|April 21, 2001
Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumoursA Agathanggelou, S Honorio, D P Macartney, 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.
European Urology|July 22, 2019
Familial Kidney Cancer: Implications of New Syndromes and Molecular InsightsMaria I Carlo, A Ari Hakimi, Grant D Stewart, 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.
Human Genetics|October 18, 2002
A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24Neil V Morgan, Paul Gissen, Saghira Malik Sharif, et al.
Neurogenetics|April 15, 2010
Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafishLaura Southgate, Dimitra Dafou, Jacqueline Hoyle, et al.
Blood|December 1, 1996
Tacrolimus and minidose methotrexate for prevention of acute graft-versus-host disease after matched unrelated donor marrow transplantationD Przepiorka, C Ippoliti, I Khouri, et al.
Human Mutation|March 25, 2009
Genetic and epigenetic analysis of recurrent hydatidiform moleBruce E Hayward, Michel De Vos, Nargese Talati, et al.
Endocrine-Related Cancer|October 21, 2010
Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibilityDewi Astuti, Christopher J Ricketts, Rasheduzzaman Chowdhury, et al.
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