- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2407
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Pancreatic cancer as a sentinel for hereditary cancer predisposition ; volume:18 ; number:1 ; day:27 ; month:6 ; year:2018 ; pages:1-9 ; date:12.2018
BMC cancer ; 18, Heft 1 (27.6.2018), 1-9, 12.2018
- Creator
-
Young, Erin L.
- Contributor
-
Thompson, Bryony A.
Neklason, Deborah W.
Firpo, Matthew A.
Werner, Theresa
Bell, Russell
Berger, Justin
Fraser, Alison
Gammon, Amanda
Koptiuch, Cathryn
Kohlmann, Wendy K.
Neumayer, Leigh
Goldgar, David E.
Mulvihill, Sean J.
Cannon-Albright, Lisa A.
Tavtigian, Sean V.
SpringerLink (Online service)
- DOI
-
10.1186/s12885-018-4573-5
- URN
-
urn:nbn:de:101:1-2018090219192750027888
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Young, Erin L.
- Thompson, Bryony A.
- Neklason, Deborah W.
- Firpo, Matthew A.
- Werner, Theresa
- Bell, Russell
- Berger, Justin
- Fraser, Alison
- Gammon, Amanda
- Koptiuch, Cathryn
- Kohlmann, Wendy K.
- Neumayer, Leigh
- Goldgar, David E.
- Mulvihill, Sean J.
- Cannon-Albright, Lisa A.
- Tavtigian, Sean V.
- SpringerLink (Online service)
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Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients
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First evidence of a large CHEK2 duplication involved in cancer predisposition in an Italian family with hereditary breast cancer
Prevalence of cancer predisposition germline variants in male breast cancer patients: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Puzzling phenomenon: adult-onset cancer predisposition and pediatric cancer
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Hereditary pancreatic cancer
Pancreatic cancer risk in hereditary pancreatitis
Surgical aspects related to hereditary pancreatic cancer
Hereditary pancreatic cancer: related syndromes and clinical perspective
Diagnostic microarray test for a genetic predisposition to hereditary nonpolyposis colorectal cancer (HNPCC)
Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients
Cancer predisposition genes in cancer-free families
First evidence of a large CHEK2 duplication involved in cancer predisposition in an Italian family with hereditary breast cancer
Prevalence of cancer predisposition germline variants in male breast cancer patients: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Puzzling phenomenon: adult-onset cancer predisposition and pediatric cancer
Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers
A second hereditary cancer predisposition syndrome in a patient with lynch syndrome and three primary cancers
Hereditary pancreatic cancer
Pancreatic cancer risk in hereditary pancreatitis
Surgical aspects related to hereditary pancreatic cancer
Hereditary pancreatic cancer: related syndromes and clinical perspective
Diagnostic microarray test for a genetic predisposition to hereditary nonpolyposis colorectal cancer (HNPCC)
Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients
Cancer predisposition genes in cancer-free families
First evidence of a large CHEK2 duplication involved in cancer predisposition in an Italian family with hereditary breast cancer
Prevalence of cancer predisposition germline variants in male breast cancer patients: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Puzzling phenomenon: adult-onset cancer predisposition and pediatric cancer
Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers