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European Journal of Pediatrics|April 17, 1999
Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhoodS Verhoef, R van Diemen-Steenvoorde, W L Akkersdijk, et al.American Journal of Human Genetics|May 20, 1999
High rate of mosaicism in tuberous sclerosis complexS Verhoef, L Bakker, A M Tempelaars, et al.Breast Cancer Research and Treatment|February 3, 2011
A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patientsM A Didraga, E H van Beers, S A Joosse, et al.Journal of Medical Genetics|January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexR Vrtel, S Verhoef, K Bouman, et al.Familial Cancer|July 27, 2010
Regular surveillance for Li-Fraumeni Syndrome: advice, adherence and perceived benefitsC R M Lammens, E M A Bleiker, N K Aaronson, et al.Familial Cancer|February 22, 2015
Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON studyM R Wevers, M K Schmidt, E G Engelhardt, et al.Familial Cancer|February 17, 2016
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriersZ Ghorbanoghli, M H Nieuwenhuis, J J Houwing-Duistermaat, et al.Clinical Genetics|February 27, 2010
Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distressC R M Lammens, E M A Bleiker, S Verhoef, et al.Journal of Medical Genetics|September 6, 2005
Cancer risks in BRCA2 families: estimates for sites other than breast and ovaryC J van Asperen, R M Brohet, E J Meijers-Heijboer, et al.Psycho-Oncology|March 9, 2011
Distress in partners of individuals diagnosed with or at high risk of developing tumors due to rare hereditary cancer syndromesC R M Lammens, E M A Bleiker, S Verhoef, et al.Pageof 4