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Journal of Medical Genetics|March 21, 2007
Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screeningS Sharif, A Moran, S M Huson, et al.Clinical Genetics|June 17, 2008
Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutationsE Barrow, W Alduaij, L Robinson, et al.Clinical Genetics|December 9, 2009
Further genotype--phenotype correlations in neurofibromatosis 2S K Selvanathan, A Shenton, R Ferner, et al.Clinical Genetics|October 10, 2006
Inherited association of breast and colorectal cancer: limited role of CHEK2 compared with high-penetrance genesH Naseem, J Boylan, D Speake, et al.Journal of Medical Genetics|February 20, 2007
Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplificationD Gareth R Evans, R T Ramsden, A Shenton, et al.Journal of Medical Genetics|June 3, 2004
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPROD G R Evans, D M Eccles, N Rahman, et al.Journal of Medical Genetics|November 3, 2006
Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screeningA Smith, A Moran, M C Boyd, et al.European Journal of Cancer (Oxford, England : 1990)|June 6, 2006
Screening younger women with a family history of breast cancer--does early detection improve outcome?A Maurice, D G R Evans, A Shenton, et al.Journal of Medical Genetics|April 17, 2008
Screening for familial ovarian cancer: poor survival of BRCA1/2 related cancersD G Evans, K N Gaarenstroom, D Stirling, et al.Journal of Medical Genetics|April 17, 2008
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinicsA C Antoniou, R Hardy, L Walker, et al.Pageof 3