Works matching IS 17312302 AND DT 2020 AND VI 18 AND IP 1
Results: 25
Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00159-6
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- Publication type:
- Article
Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in Singapore.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00156-9
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- Publication type:
- Article
Metachronous cutaneous squamous cell carcinoma in a young patient as the only presenting symptom to uncover Lynch syndrome with MLH1 Germline mutation.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00155-w
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- Publication type:
- Article
An in-depth exploration of the post-test informational needs of BRCA1 and BRCA2 pathogenic variant carriers in Asia.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00154-x
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- Publication type:
- Article
Biological and clinical impact of central nervous system hemangioblastomas in Chinese patients with von Hippel-Lindau disease: implications for treatment.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00153-y
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- Publication type:
- Article
Preferences for breast cancer prevention among women with a BRCA1 or BRCA2 mutation.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00152-z
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- Publication type:
- Article
Patients with unexplained mismatch repair deficiency are interested in updated genetic testing.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. N.PAG, doi. 10.1186/s13053-020-00150-1
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- Publication type:
- Article
Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00151-0
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- Publication type:
- Article
Retrospective review of outcomes in patients with DNA-damage repair related pancreatic cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00148-9
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- Publication type:
- Article
Polymorphisms in MMP-1, MMP-2, MMP-7, MMP-13 and MT2A do not contribute to breast, lung and colon cancer risk in polish population.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00147-w
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- Publication type:
- Article
Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00146-x
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- Publication type:
- Article
An American patient with polyposis carrying a Scandinavian AXIN2 pathogenic variant.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Adherence to National Comprehensive Cancer Network Guidelines for BRCA testing among high risk breast Cancer patients: a retrospective chart review study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00144-z
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- Publication type:
- Article
Increased risk for uterine cancer among first-degree relatives to Swedish gastric cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00145-y
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- Publication type:
- Article
Correction to: Expectations and psychological issues before genetic counseling: analysis of distress determinant factors.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Expectations and psychological issues before genetic counseling: analysis of distress determinant factors.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00142-1
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- Publication type:
- Article
Development and validation of next generation sequencing based 35-gene hereditary cancer panel.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00141-2
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- Publication type:
- Article
A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00140-3
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- Publication type:
- Article
An interesting case of likely BRCA2 related bilateral breast cancer with metastasis in the fimbrial part of fallopian tube.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00139-w
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- Publication type:
- Article
The Prospective Lynch Syndrome Database reports enable evidence-based personal precision health care.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0138-0
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- Publication type:
- Article
Diet, weight management, physical activity and Ovarian & Breast Cancer Risk in women with BRCA1/2 pathogenic Germline gene variants: systematic review.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0137-1
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- Publication type:
- Article
Ubiquitous neurocognitive dysfunction in familial adenomatous polyposis: proof-of-concept of the role of APC protein in neurocognitive function.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0135-3
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- Publication type:
- Article
Group plus "mini" individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0136-2
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- Publication type:
- Article
On the road with Henry Lynch.
- Published in:
- 2020
- By:
- Publication type:
- Editorial
Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-0133-5
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- Publication type:
- Article