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1.
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome.
J Transl Med
; 21(1): 282, 2023 04 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-37101184
2.
Lynch syndrome testing of colorectal cancer patients in a high-income country with universal healthcare: a retrospective study of current practice and gaps in seven australian hospitals.
Hered Cancer Clin Pract
; 20(1): 18, 2022 May 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35509103
3.
Lynch syndrome associated endometrial carcinomas in Western Australia: an analysis of universal screening by mismatch repair protein immunohistochemistry.
Int J Gynecol Cancer
; 31(6): 846-851, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33858951
4.
Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice.
Hered Cancer Clin Pract
; 19(1): 24, 2021 Apr 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33836815
5.
Uptake of testing for germline BRCA mutations in patients with non-mucinous epithelial ovarian cancers in Western Australia: a comparison of different genetic counseling methods.
Int J Gynecol Cancer
; 29(6): 1038-1042, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31101686
6.
Prognostic Role of Histological Tumor Regression in Patients Receiving Neoadjuvant Chemotherapy for High-Grade Serous Tubo-ovarian Carcinoma.
Int J Gynecol Cancer
; 27(4): 708-713, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28441251
7.
Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing.
Int J Gynecol Cancer
; 26(5): 892-7, 2016 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-27051053
8.
Assessing the effects of a drought experiment on the reproductive phenology and ecophysiology of a wet tropical rainforest community.
Conserv Physiol
; 11(1): coad064, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37732160
9.
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study.
J Community Genet
; 14(3): 307-317, 2023 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-37012465
10.
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands.
Cancers (Basel)
; 15(20)2023 Oct 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37894291
11.
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome.
medRxiv
; 2023 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36909643
12.
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants-a multi-site prospective cohort study.
Genome Med
; 15(1): 74, 2023 09 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-37723522
13.
Opinions and experiences of recontacting patients: a survey of Australasian genetic health professionals.
J Community Genet
; 13(2): 193-199, 2022 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-35013911
14.
Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study.
J Community Genet
; 13(1): 59-73, 2022 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-34727336
15.
TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.
J Clin Oncol
; 40(18): 2036-2047, 2022 06 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-35263119
16.
Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.
Patient Educ Couns
; 101(5): 938-944, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29273311
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