Works matching IS 17312302 AND DT 2018 AND VI 16
Results: 17
German National Case Collection for familial pancreatic Cancer (FaPaCa) - acceptance and psychological aspects of a pancreatic cancer screening program.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0100-6
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- Publication type:
- Article
A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0098-9
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- Publication type:
- Article
Polyglobulia in patients with hemangioblastomas is related to tumor size but not to serum erythropoietin.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0097-x
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- Publication type:
- Article
CD36 – a plausible modifier of disease phenotype in familial adenomatous polyposis.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0096-y
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- Publication type:
- Article
A qualitative study of barriers to genetic counseling and potential for mobile technology education among women with ovarian cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0095-z
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- Publication type:
- Article
High frequency of pathogenic non-founder germline mutations in <italic>BRCA1</italic> and <italic>BRCA2</italic> in families with breast and ovarian cancer in a founder population.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0094-0
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- Publication type:
- Article
Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0090-4
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- Publication type:
- Article
Retraction Note to: The <italic>BRCA2</italic> variant c.68–7 T > A is associated with breast cancer.
- Published in:
- 2018
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- Publication type:
- Correction Notice
Platinum-based neoadjuvant chemotherapy in BRCA1-positive breast cancer: a retrospective cohort analysis and literature review.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0092-2
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- Publication type:
- Article
Challenges in recruiting African-American women for a breast cancer genetics study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0091-3
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- Publication type:
- Article
CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome.
- Published in:
- 2018
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- Publication type:
- Case Study
Clinical Genetics of Cancer 2017.
- Published in:
- 2018
- Publication type:
- Abstract
Frequency of <italic>BRCA1</italic> and <italic>BRCA2</italic> causative founder variants in ovarian cancer patients in South-East Poland.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-018-0089-x
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- Publication type:
- Article
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-018-0086-0
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- Publication type:
- Article
BRCA1 and BRCA2 mutation spectrum -- an update on mutation distribution in a large cancer genetics clinic in Norway.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0085-6
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- Publication type:
- Article
Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0084-7
- By:
- Publication type:
- Article
Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0083-8
- By:
- Publication type:
- Article