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Editions published in Familial Cancer 200
Too many entities requested (1282). Only 200 are displayed.
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Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls
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A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.
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Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas
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The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial cases
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Determining the familial risk distribution of colorectal cancer: a data mining approach.
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Birt-Hogg-Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas.
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Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study.
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The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety
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A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine
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Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study
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Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women
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Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk
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Familial and sporadic pancreatic cancer share the same molecular pathogenesis
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Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews
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High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations.
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POLE mutations in families predisposed to cutaneous melanoma
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Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients
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Germline TERT promoter mutations are rare in familial melanoma
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Diagnostic values of osteopontin combined with CA125 for ovarian cancer: a meta-analysis
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Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.
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Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer
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The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significance
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Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome
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Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers
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Prevalence and detection of psychosocial problems in cancer genetic counseling
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The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy
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Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.
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Childhood cancers in families with and without Lynch syndrome
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Genetic testing for Lynch syndrome: family communication and motivation
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Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary
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Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry
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Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis
Subject - wd:Q15761917