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Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|February 1, 2020
A randomized trial comparing vascular access strategies for patients receiving chemotherapy with trastuzumab for early-stage breast cancerMark Clemons, Carol Stober, Anne Kehoe, et al.
Oncogene|March 16, 2002
Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancerTimothy R Porter, Frances M Richards, Richard S Houlston, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|May 25, 2022
Using machine learning to predict individual patient toxicities from cancer treatmentsKatherine Marie Cole, Mark Clemons, Sharon McGee, et al.
Breast Cancer Research and Treatment|August 9, 2019
A multicentre, randomized pilot trial comparing vascular access strategies for early stage breast cancer patients receiving non-trastuzumab containing chemotherapyAndrew Robinson, Carol Stober, Dean Fergusson, et al.
European Journal of Human Genetics : EJHG|July 7, 2005
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndromeWendy N Cooper, Anita Luharia, Gail A Evans, et al.
Human Mutation|October 6, 2009
A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) geneDerek H K Lim, Pauline K Rehal, Michael S Nahorski, et al.
Journal of Medical Genetics|December 15, 2011
CHRNG genotype-phenotype correlations in the multiple pterygium syndromesJulie Vogt, Neil V Morgan, Pauline Rehal, et al.
Oncogene|October 14, 2003
Multigene methylation analysis of Wilms' tumour and adult renal cell carcinomaMark R Morris, Luke B Hesson, Kate J Wagner, et al.
Molecular Genetics and Metabolism|March 16, 2010
Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: implications for molecular diagnosisDanielle Crompton, Pauline K Rehal, Lesley MacPherson, et al.
European Journal of Human Genetics : EJHG|November 16, 2006
Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10Dominic R A White, Anuradha Ganesh, Darryl Nishimura, et al.
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