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Foreword | |
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Preface | |
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Acknowledgments | |
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Cancer Epidemiology | |
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Cancer Statistics | |
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Cancer Etiology | |
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Case Examples | |
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Further Reading | |
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Cancer Detection and Treatment | |
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The Diagnosis of Cancer | |
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Tumor Classification | |
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Cancer Treatment | |
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Further Reading | |
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Cancer Biology | |
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The Malignant Cell | |
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Carcinogenesis | |
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Oncogenes | |
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Tumor Suppressor Genes | |
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Epigenetic Mechanisms | |
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Further Reading | |
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Hereditary Cancer Syndromes | |
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Ataxia Telangiectasia | |
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Autoimmune Lymphoproliferative Syndrome (Also Canale-Smith Syndrome) | |
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Beckwith-Wiedemann Syndrome (Also Exomphalos Macroglossia Gigantism [EMG] Syndrome) | |
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Birt-Hogg-Dub� Syndrome | |
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Bloom Syndrome | |
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Blue Rubber Bleb Nevus Syndrome (Also Termed Bean Syndrome) | |
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Breast-Ovarian Cancer Syndrome, Hereditary | |
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Carney Complex, Types I and II (Includes NAME Syndrome and LAMB Syndrome) | |
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Diamond-Blackfan Anemia | |
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Familial Adenomatous Polyposis (Also Attenuated FAP, Gardner's Syndrome, Turcot Syndrome, and Hereditary Desmoid Disease) | |
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Fanconi Anemia | |
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Gastric Cancer, Hereditary Diffuse | |
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Gastrointestinal Stromal Tumor, Familial (Also Multiple GI Autonomic Nerve Tumors) | |
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Juvenile Polyposis (Includes Hereditary Mixed Polyposis) | |
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Leiomyomatosis Renal Cell Cancer, Hereditary | |
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Li-Fraumeni Syndrome | |
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Lynch Syndrome (Also Termed HNPCC) | |
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Melanoma, Cutaneous Malignant (Includes Familial Atypical Mole-Malignant Melanoma Syndrome, Dysplastic Nevus Syndrome, and Melanoma-Astrocytoma Syndrome) | |
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Multiple Endocrine Neoplasia, Type 1 (Also Wermer Syndrome) | |
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Multiple Endocrine Neoplasia, Type 2 (Also Sipple Syndrome, Familial Medullary Thyroid Carcinoma Syndrome) | |
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MYH-Associated Polyposis | |
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Neuroblastoma, Familial | |
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Neurofibromatosis, Type 1 (Also von Recklinghausen Disease) | |
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Neurofibromatosis, Type 2 | |
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Nevoid Basal Cell Carcinoma Syndrome (Also Gorlin Syndrome, Basal Cell Nevus Syndrome) | |
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Paraganglioma-Pheochromocytoma Syndrome, Hereditary (Including Carney-Stratakis Syndrome) | |
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Peutz-Jeghers Syndrome | |
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PTEN Hamartoma Syndrome (PHS) (Also Cowden Syndrome; Includes Bannayan-Riley-Ruvalcaba Syndrome and Proteus Syndrome) | |
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Renal Cell Carcinoma, Hereditary Papillary | |
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Retinoblastoma, Hereditary | |
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Rothmund-Thomson Syndrome | |
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Tuberous Sclerosis Complex (TSC) | |
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Von Hippel Lindau Syndrome | |
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Werner Syndrome (Also Termed Progeria of the Adult) | |
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Wilms Tumor, Familial (Includes Denys-Drash Syndrome, Frasier Syndrome, WAGR Syndrome) | |
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Xeroderma Pigmentosum (Includes XP/CS Complex, XP Variant) | |
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Further Reading | |
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All About Breast Cancer | |
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Overview of Breast Cancer | |
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Breast Cancer Management: Screening, Diagnosis, and Treatment | |
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Breast Cancer Syndromes | |
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Further Reading | |
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All About Colorectal Cancer | |
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Overview of Colorectal Cancer | |
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CRC Management: Screening, Diagnosis, and Treatment | |
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CRC Syndromes | |
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Further Reading | |
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Collecting and Interpreting Cancer Histories | |
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Collecting a Cancer History | |
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Challenges to Collecting an Accurate History | |
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Interpreting a Cancer History | |
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Case Examples | |
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Further Reading | |
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Cancer Risk Communication | |
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Genetic Counseling and Risk Perception | |
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The Communication of Risk | |
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Counseling Clients at various Risks | |
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Case Examples | |
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Further Reading | |
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Genetic Testing and Counseling | |
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The Logistics of Arranging Tests | |
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Pretest Counseling | |
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Results Disclosure and Follow-Up | |
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Case Examples | |
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Further Reading | |
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Psychosocial Aspects of Cancer Counseling | |
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The Psychosocial Features of Clients | |
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Making a Psychosocial Assessment | |
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Providing Additional Emotional Support | |
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Case Examples | |
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Further Reading | |
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Ethical Issues in Cancer Genetic Counseling | |
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Bioethical Principles and Guidelines | |
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Strategies for Resolving Ethical Dilemmas | |
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Types of Ethical Dilemmas in Cancer Genetic Counseling | |
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Issues of Justice | |
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Further Reading | |
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Specific Tumor Types and Associated Syndromes | |
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Review of Basic Pedigree Symbols | |
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Index | |