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BMC Cancer
|
January 17, 2014
The efficacy of a standardized questionnaire in facilitating personalized communication about problems encountered in cancer genetic counseling: design of a randomized controlled trial
Willem Eijzenga, Neil K Aaronson, Irma Kluijt, et al.
The Journal of Pathology
|
August 21, 2018
Ethical considerations for modern molecular pathology
Shoko Vos, Paul J van Diest, Margreet Gem Ausems, et al.
European Journal of Human Genetics : EJHG
|
April 14, 2016
Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered
Rhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners
|
October 24, 2018
Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care
Charles W Helsper, Liesbeth M Van Vliet, Mary E Velthuizen, et al.
Hereditary Cancer in Clinical Practice
|
August 14, 2010
A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
Els van Riel, Margreet Gem Ausems, Frans Bl Hogervorst, et al.
Breast Cancer Research : BCR
|
December 1, 2010
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers
Logan C Walker, Zachary S Fredericksen, Xianshu Wang, et al.
British Journal of Cancer
|
January 5, 2018
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition
Christos Mikropoulos, Christina G Hutten Selkirk, Sibel Saya, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
BMC Cancer
|
January 17, 2014
The efficacy of a standardized questionnaire in facilitating personalized communication about problems encountered in cancer genetic counseling: design of a randomized controlled trial
Willem Eijzenga, Neil K Aaronson, Irma Kluijt, et al.
The Journal of Pathology
|
August 21, 2018
Ethical considerations for modern molecular pathology
Shoko Vos, Paul J van Diest, Margreet Gem Ausems, et al.
European Journal of Human Genetics : EJHG
|
April 14, 2016
Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered
Rhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners
|
October 24, 2018
Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care
Charles W Helsper, Liesbeth M Van Vliet, Mary E Velthuizen, et al.
Hereditary Cancer in Clinical Practice
|
August 14, 2010
A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome
Els van Riel, Margreet Gem Ausems, Frans Bl Hogervorst, et al.
Breast Cancer Research : BCR
|
December 1, 2010
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers
Logan C Walker, Zachary S Fredericksen, Xianshu Wang, et al.
British Journal of Cancer
|
January 5, 2018
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition
Christos Mikropoulos, Christina G Hutten Selkirk, Sibel Saya, et al.
Page
of 1