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1.
The risk of skin cancer in women who carry BRCA1 or BRCA2 mutations.
Hered Cancer Clin Pract
; 22(1): 7, 2024 May 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-38741145
2.
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings.
Hum Genet
; 141(12): 1875-1885, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-35739291
3.
Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers.
Pediatr Blood Cancer
; 68(8): e29021, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33788392
4.
Setting a baseline: A 7-year review of referral rates and outcomes for serous ovarian cancer prior to implementation of oncologist mediated genetic testing.
Gynecol Oncol
; 158(2): 440-445, 2020 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-32505554
5.
Accreditation Council for Genetic Counseling Board of Directors Response to Myers et al 'A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination'.
J Genet Couns
; 31(2): 316-318, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35150179
6.
All in the Family: Barriers and Motivators to the Use of Cancer Family History Questionnaires and the Impact on Attendance Rates.
J Genet Couns
; 24(5): 822-32, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25558824
7.
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.
BMJ Open
; 12(4): e060899, 2022 04 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-35487723
8.
The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population.
J Genet Couns
; 20(4): 355-64, 2011 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-21448763
9.
Breast and ovarian cancer: the forgotten paternal contribution.
J Genet Couns
; 20(5): 442-9, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21503821
10.
A Comparison of Patient-Reported Outcomes Following Consent for Genetic Testing Using an Oncologist- or Genetic Counselor-Mediated Model of Care.
Curr Oncol
; 28(2): 1459-1471, 2021 04 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33917963
11.
Incidental findings from cancer next generation sequencing panels.
NPJ Genom Med
; 6(1): 63, 2021 Jul 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-34282142
12.
The effectiveness of family history questionnaires in cancer genetic counseling.
J Genet Couns
; 18(4): 366-78, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19459037
13.
Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
BMJ Open
; 9(10): e031092, 2019 10 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31594892
14.
Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
Cancers (Basel)
; 10(11)2018 Nov 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-30428547
15.
Breast and ovarian cancer: Y do we forget about dad?
Lancet Oncol
; 11(12): 1115-7, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-20971682
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