Works matching IS 17312302 AND DT 2019 AND VI 17 AND IP 1
Results: 32
A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0126-4
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- Article
Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0125-5
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- Article
Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0120-x
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- Article
Colorectal carcinoma in the course of inflammatory bowel diseases.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0118-4
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- Article
Serum selenium level and cancer risk: a nested case-control study.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0131-7
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- Article
Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0132-6
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- Article
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0130-8
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- Article
Genetic counselling and personalised risk assessment in the Australian pancreatic cancer screening program.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0129-1
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- Article
Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0128-2
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- Article
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0127-3
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- Article
Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0122-8
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- Article
Somatic variants of potential clinical significance in the tumors of BRCA phenocopies.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0117-5
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- Article
Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0119-3
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- Article
Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0123-7
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- Article
Germline c.1A>C heterozygous pathogenic variant in SDHA reported for the first time in a young adult with a gastric gastrointestinal stromal tumour (GIST): a case report.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0124-6
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A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0121-9
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- Article
Allelic variants of breast cancer susceptibility genes PALB2 and RECQL in the Latvian population.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0116-6
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- Article
Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0114-8
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- Article
Single-center study of Lynch syndrome screening in colorectal polyps.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0108-6
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- Article
BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0107-7
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- Article
Endometrioid endometrial cancer "recurring" as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0112-x
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- Article
The effect of neoadjuvant platinum-based chemotherapy in BRCA mutated triple negative breast cancers -systematic review and meta-analysis.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0111-y
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Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0113-9
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- Article
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0106-8
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Meeting abstracts from the Annual Conference Clinical Genetics of Cancer 2018.
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- 2019
- Publication type:
- Calendar
Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0110-z
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Selected features of breast and peritoneal cancers diagnosed in BRCA1 carriers after risk-reducing salpingo-oophorectomy.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0109-5
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BRCA mutation screening and patterns among high-risk Lebanese subjects.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0105-9
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- Article
Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS).
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0104-x
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Validation of a digital identification tool for individuals at risk for hereditary cancer syndromes.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0099-8
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- Article
The association between non-breast and ovary cancers and BRCA mutation in first- and second-degree relatives of high-risk breast cancer patients: a large-scale study of Koreans.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0103-3
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Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0102-4
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- Article