Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27474
Title: Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants.
Austin Authors: Murali, Krithika;Dwarte, Tanya M;Nikfarjam, Mehrdad ;Tucker, Katherine M;Vaughan, Rhys B ;Efthymiou, Marios ;Collins, Allison L ;Spigelman, Allan D;Salmon, Lucinda ;Johns, Amber L;Williams, David B;Delatycki, Martin B ;John, Thomas ;Stoita, Alina
Affiliation: Cancer Genetics Unit, The Kinghorn Cancer Centre, St Vincent's Hospital, Darlinghurst, NSW, 2010, Australia
Gastroenterology and Hepatology
Olivia Newton-John Cancer Wellness and Research Centre
Department of Gastroenterology, St Vincent's Hospital, Darlinghurst, NSW, 2010, Australia
University of New South Wales, St Vincent's Clinical School and Prince of Wales Clinical School, Randwick, NSW, 2031, Australia
Clinical Genetics
Australian Pancreatic Cancer Genome Initiative, Garvan Institute of Medical Research, Darlinghurst, NSW, 2010, Australia
Peter MacCallum Cancer Centre, Parkville, VIC, 3000, Australia
Hereditary Cancer Centre, Prince of Wales Hospital, Randwick, NSW, 2031, Australia
Surgery
Issue Date: 8-Sep-2021
Date: 2021-09-08
Publication information: Hereditary Cancer in Clinical Practice 2021; 19(1): 37
URI: https://ahro.austin.org.au/austinjspui/handle/1/27474
DOI: 10.1186/s13053-021-00195-w
Journal: Hereditary Cancer in Clinical Practice
PubMed URL: 34496934
ISSN: 1731-2302
Type: Journal Article
Appears in Collections:Journal articles

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