Should physicians warn patients' relatives of genetic risks?

scientific article

Should physicians warn patients' relatives of genetic risks? is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1503/CMAJ.070956
P8608Fatcat IDrelease_i4txnqziurbk7hh6tfijknjgnq
P932PMC publication ID2244654
P698PubMed publication ID18299550
P5875ResearchGate publication ID5551927

P50authorBartha KnoppersQ2885924
Béatrice GodardQ87810516
P2093author name stringGillian Nycum
Mireille Lacroix
P2860cites workGuidelines for disclosing genetic information to family members: from development to use.Q36417821
Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutationQ36754871
Genetic information and the family: are we our brother's keeper?Q45258337
P433issue5
P407language of work or nameEnglishQ1860
P304page(s)593-595
P577publication date2008-02-01
P1433published inCanadian Medical Association JournalQ5030320
P1476titleShould physicians warn patients' relatives of genetic risks?
P478volume178

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cites work (P2860)
Q28602727'Is this knowledge mine and nobody else's? I don't feel that.' Patient views about consent, confidentiality and information-sharing in genetic medicine
Q372909562012 European thyroid association guidelines for genetic testing and its clinical consequences in medullary thyroid cancer
Q37435858Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.
Q56774558Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent
Q35620233Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?
Q34326743Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information
Q35855495Getting a head start: the importance of personal genetics education in high schools
Q57947268Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
Q36884609Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider
Q38819370Leveling the Playing Field: Closing the Gap in Public Awareness of Genetics between the Well Served and Underserved
Q56775340Paediatric biobanks: what makes them so unique?
Q37831280Parental views on tissue banking in pediatric oncology patients
Q38611712Population genetic testing for cancer susceptibility: founder mutations to genomes
Q36164685Preconception care and genetic risk: ethical issues
Q88917800The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice
Q48470406Whole-genome sequencing and the physician

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