Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland.
- DOI
- 10.1186/s13053-018-0089-x
- Published
- 2018
- Container
- Hereditary cancer in clinical practice
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- supportingOpen access status: Normalized open-access status: open.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1186/s13053-018-0089-x,
title = {Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland.},
author = {Kluz T and Jasiewicz A and Marczyk E and Jach R and Jakubowska A and Lubiński J and Narod SA and Gronwald J},
year = {2018},
journal = {Hereditary cancer in clinical practice},
doi = {10.1186/s13053-018-0089-x},
url = {https://doi.org/10.1186/s13053-018-0089-x}
}RIS
TY - JOUR TI - Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland. AU - Kluz T AU - Jasiewicz A AU - Marczyk E AU - Jach R AU - Jakubowska A AU - Lubiński J AU - Narod SA AU - Gronwald J PY - 2018 JO - Hereditary cancer in clinical practice DO - 10.1186/s13053-018-0089-x UR - https://doi.org/10.1186/s13053-018-0089-x ER -
APA
T, K., A, J., E, M., R, J., A, J., J, L., SA, N., & J, G. (2018). Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland.. Hereditary cancer in clinical practice. https://doi.org/10.1186/s13053-018-0089-x
Source records
- pubmed · retrieved 2026-09-26T13:58:32.731Z