Colorectal carcinoma in the course of inflammatory bowel diseases
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0118-4
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
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0106-8
The effect of neoadjuvant platinum-based chemotherapy in BRCA mutated triple negative breast cancers -systematic review and meta-analysis
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0111-y
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0127-3
Increased breast cancer risk in women with neurofibromatosis type 1: a meta-analysis and systematic review of the literature
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0110-z
Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0125-5
BRCA mutation screening and patterns among high-risk Lebanese subjects
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0105-9
Single-center study of Lynch syndrome screening in colorectal polyps
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0108-6
Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-018-0102-4
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
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-018-0103-3
A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0121-9
Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0120-x
Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0119-3
Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0114-8
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)
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0104-x
Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0113-9
Validation of a digital identification tool for individuals at risk for hereditary cancer syndromes
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-018-0099-8
Genetic counselling and personalised risk assessment in the Australian pancreatic cancer screening program
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0129-1
Somatic variants of potential clinical significance in the tumors of BRCA phenocopies
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0117-5
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0130-8
Serum selenium level and cancer risk: a nested case-control study
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0131-7
Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0128-2
Allelic variants of breast cancer susceptibility genes PALB2 and RECQL in the Latvian population
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0116-6
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?
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0112-x
BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0107-7
Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0123-7
Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0132-6
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
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0124-6
Selected Abstracts from the 3rd European Hereditary Tumour Group Meeting (EHTG 2018)
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0115-7
Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0122-8
A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0126-4
Selected features of breast and peritoneal cancers diagnosed in BRCA1 carriers after risk-reducing salpingo-oophorectomy
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-019-0109-5
Meeting abstracts from the Annual Conference Clinical Genetics of Cancer 2018
来源期刊:Hereditary Cancer in Clinical PracticeDOI:10.1186/s13053-018-0101-5