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المؤلفون: Nieuwenhuis, M.H., Kets, C.M., Murphy-Ryan, M., Colas, C., Moller, P., Hes, F.J., Hodgson, S.V., Olderode-Berends, M.J.W., Aretz, S., Heinimann, K., Gomez Garcia, E.B., Douglas, F., Spigelman, A., Timshel, S., Lindor, N.M., Vasen, H.F.A.
المساهمون: Faculty of Physical Education and Physical Therapy, Clinical sciences, Medical Genetics, Klinische Genetica, Genetica & Celbiologie, RS: GROW - School for Oncology and Reproduction
المصدر: Colorectal Disease, 14, 9, pp. e562-6
Colorectal Disease, 14, e562-6
Colorectal Disease, 14(9), e562-e566. Wileyمصطلحات موضوعية: Adult, Male, Adolescent, Child, preschool, Kaplan-Meier Estimate, DISEASE, COWDEN-SYNDROME, Humans, Genetic Predisposition to Disease, Child, Colorectal Neoplasms/etiology, Germ-Line Mutation, Aged, Hereditary cancer and cancer-related syndromes [ONCOL 1], multiple hamartoma syndrome, Infant, PTEN Phosphohydrolase/genetics, Middle Aged, colorectal neoplasms, CANCER, Hamartoma Syndrome, Multiple/complications, CARCINOMAS, Cohort studies, Colonic Polyps/etiology, Female, PTEN phosphohydrolase, HAMARTOMATOUS POLYPOSIS SYNDROMES