To the Seminar --;Aetiology and Epidemiology --;Markovian Models as a Tool in Epidemiology --;Familial Adenomatous Polyposis: Current Status in Switzerland --;Down-Regulation of a Cell-Surface Glycoprotein Correlated with Rearrangement of Chromosome 1 in Human Breast Cancer Cells --;Gastric Cancer in Hawaii Japanese: A Family Study --;Increased Number of Multiple Melanomas in Sporadic and Familial Variants of Dysplastic Naevus Syndrome --;Family History in Clinical Trials: Experience of the IBCSG and the SAKK --;Aetiology and Epidemiology --;Report of Rapporteur --;Lynch Syndromes --;Lynch Syndromes I and II --;Natural History, Diagnosis and Control Strategies --;Cost-Benefit Implications in the Surveillance of Lynch Syndrome Subjects --;Treatment --;Is Endoscopy Still Controversial in Secondary Prevention of Colon Cancer? --;Preventive Surgery --;Desmoids in Gardner's Syndrome: A Challenge for Surgeons --;Radiation and Cancer Prevention --;Chemoprevention --;Familial Cancer Control --;Cancer Prevention Through Genetic Counselling --;Identification of Persons at High Risk for Cancer: A Delay in UV-lnduced DNA Repair is Correlated with Multiple Skin Cancer --;The Nurse's Role in Familial Cancer --;Screening for Colorectal Neoplasia in Families --;Risk Assessment in Hereditary Breast Cancer --;A Screening Programme for Medullary Thyroid Carcinoma and Breast Cancer for Families at High Risk --;Familial Cancer Control --;Report of Rapporteur --;A Clinical Study of Familial Cancer in Japan --;DNA Diagnosis in Families with Hereditary Forms of Cancer --;UICC Strategy Meeting --;Familial Cancer Among Cancer Patients Registered at the Aichi Cancer Registry --;Heterogeneity of Aggregation of Familial Cancer --;Report of the First UICC Strategy Meeting on Familial Cancer.
یادداشتهای مربوط به خلاصه یا چکیده
متن يادداشت
This monograph contains the contributions of a seminar on familial cancer. All types of cancer show a tendency to aggregate in families. Cancer families can be identified by taking a family history in cancer patients. This method is useful for detecting cancer genes and determining which persons carry a high risk for cancer and who may thus benefit frompreventive measures such as screening and chemoprevention.
موضوع (اسم عام یاعبارت اسمی عام)
موضوع مستند نشده
Human genetics.
موضوع مستند نشده
Medicine.
موضوع مستند نشده
Oncology.
رده بندی کنگره
شماره رده
RC267
.
4
نشانه اثر
E358
1992
نام شخص به منزله سر شناسه - (مسئولیت معنوی درجه اول )