Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors.
about
Personal genomics services: whose genomes?Challenging and complex decisions in the management of the BRCA mutation carrierLamina-associated polypeptide (LAP)2α and other LEM proteins in cancer biologyThe development and analysis of tutorial dialogues in AutoTutor Lite.Genetic risk assessments in individuals at high risk for inherited breast cancer in the breast oncology care setting.BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experienceLife trajectories, genetic testing, and risk reduction decisions in 18-39 year old women at risk for hereditary breast and ovarian cancer.A monograph proposing the use of canine mammary tumours as a model for the study of hereditary breast cancer susceptibility genes in humansUse of an educational computer program before genetic counseling for breast cancer susceptibility: effects on duration and content of counseling sessions.Linking genetic counseling content to short-term outcomes in individuals at elevated breast cancer riskIdentification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian CancerDNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct.Controversies in communication of genetic screening results for cancer: a report from the American Society of Preventive Oncology's Screening Special Interest Group (ASPO's 33rd Annual Meeting, March 8 to 10, 2009, Tampa, Florida).Methodological quality of English-language genetic guidelines on hereditary breast-cancer screening and management: an evaluation using the AGREE instrument.Efficacy of a web-based intelligent tutoring system for communicating genetic risk of breast cancer: a fuzzy-trace theory approach.Support of personalized medicine through risk-stratified treatment recommendations - an environmental scan of clinical practice guidelines.Development of a communication protocol for telephone disclosure of genetic test results for cancer predispositionGenetic counselor opinions of, and experiences with telephone communication of BRCA1/2 test resultsFive skills psychiatrists should have in order to provide patients with optimal ethical care.Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec.Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial.Testicular cancer and genetics knowledge among familial testicular cancer family members.Prophylactic and Therapeutic Breast Conservation in BRCA1/2 Mutation CarriersClinical Considerations of BRCA1- and BRCA2-Mutation Carriers: A Review.Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriersEligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling.A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome.Outcomes of a systems-level intervention offering breast cancer risk assessments to low-income underserved women.Dealing with the unexpected: consumer responses to direct-access BRCA mutation testingIdentification of the prevalent BRCA1 and BRCA2 mutations in the female population of Puerto RicoExploring hereditary cancer among dying cancer patients--a cross-sectional study of hereditary risk and perceived awareness of DNA testing and banking.Management of the asymptomatic BRCA mutation carrier.Incorporating information regarding preimplantation genetic diagnosis into discussions concerning testing and risk management for BRCA1/2 mutations: a qualitative study of patient preferences.The korean hereditary breast cancer study: review and future perspectives.The effects of a genetic counseling educational program on hereditary breast cancer for korean healthcare providers.Individual breast cancer risk assessment in underserved populations: integrating empirical bioethics and health disparities research.Cognitive and psychological impact of BRCA genetic counseling in before and after definitive surgery breast cancer patients.Understanding Genetic Breast Cancer Risk: Processing Loci of the BRCA Gist Intelligent Tutoring System.The evolution of personalized cancer genetic counseling in the era of personalized medicine.Development and validation of a primary care-based family health history and decision support program (MeTree).
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P2860
Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Risk assessment and genetic co ...... Society of Genetic Counselors.
@en
type
label
Risk assessment and genetic co ...... Society of Genetic Counselors.
@en
prefLabel
Risk assessment and genetic co ...... Society of Genetic Counselors.
@en
P2093
P2860
P1476
Risk assessment and genetic co ...... Society of Genetic Counselors.
@en
P2093
Angela Musial Fay
Janice L Berliner
Practice Issues Subcommittee o ...... nseling Special Interest Group
P2860
P304
P356
10.1007/S10897-007-9090-7
P577
2007-05-17T00:00:00Z