Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 1
Results: 23
Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations.
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- Familial Cancer, 2015, v. 14, n. 1, p. 129, doi. 10.1007/s10689-014-9747-y
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- Article
Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe.
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- Familial Cancer, 2015, v. 14, n. 1, p. 145, doi. 10.1007/s10689-014-9748-x
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Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing.
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- Familial Cancer, 2015, v. 14, n. 1, p. 9, doi. 10.1007/s10689-014-9749-9
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APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes.
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- Familial Cancer, 2015, v. 14, n. 1, p. 41, doi. 10.1007/s10689-014-9750-3
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Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case.
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- Familial Cancer, 2015, v. 14, n. 1, p. 61, doi. 10.1007/s10689-014-9751-2
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Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome.
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- Familial Cancer, 2015, v. 14, n. 1, p. 151, doi. 10.1007/s10689-014-9752-1
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- Article
MLH1 promotor hypermethylation does not rule out a diagnosis of Lynch syndrome: a case report.
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- Familial Cancer, 2015, v. 14, n. 1, p. 77, doi. 10.1007/s10689-014-9753-0
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Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li-Fraumeni syndrome.
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- Familial Cancer, 2015, v. 14, n. 1, p. 161, doi. 10.1007/s10689-014-9754-z
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- Article
Familial and sporadic pancreatic cancer share the same molecular pathogenesis.
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- Familial Cancer, 2015, v. 14, n. 1, p. 95, doi. 10.1007/s10689-014-9755-y
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- Article
Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals.
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- Familial Cancer, 2015, v. 14, n. 1, p. 167, doi. 10.1007/s10689-014-9756-x
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Mitochondrial membrane potential and reactive oxygen species in cancer stem cells.
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- Familial Cancer, 2015, v. 14, n. 1, p. 19, doi. 10.1007/s10689-014-9757-9
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Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer.
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- Familial Cancer, 2015, v. 14, n. 1, p. 105, doi. 10.1007/s10689-014-9759-7
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Desmoid tumour in familial adenomatous polyposis patients: responses to treatments.
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- Familial Cancer, 2015, v. 14, n. 1, p. 31, doi. 10.1007/s10689-014-9760-1
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- Article
The impact of risk-reducing gynaecological surgery in premenopausal women at high risk of endometrial and ovarian cancer due to Lynch syndrome.
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- Familial Cancer, 2015, v. 14, n. 1, p. 51, doi. 10.1007/s10689-014-9761-0
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Down-regulation of malignant potential by alpha linolenic acid in human and mouse colon cancer cells.
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- Familial Cancer, 2015, v. 14, n. 1, p. 25, doi. 10.1007/s10689-014-9762-z
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Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review.
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- Familial Cancer, 2015, v. 14, n. 1, p. 157, doi. 10.1007/s10689-014-9763-y
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- Article
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation.
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- Familial Cancer, 2015, v. 14, n. 1, p. 89, doi. 10.1007/s10689-014-9764-x
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Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.
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- Familial Cancer, 2015, v. 14, n. 1, p. 69, doi. 10.1007/s10689-014-9765-9
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- Article
Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability.
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- Familial Cancer, 2015, v. 14, n. 1, p. 117, doi. 10.1007/s10689-014-9766-8
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- Article
Single nucleotide polymorphisms in PDCD6 gene are associated with the development of cervical squamous cell carcinoma.
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- Familial Cancer, 2015, v. 14, n. 1, p. 1, doi. 10.1007/s10689-014-9767-7
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18th annual meeting: Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA-ICC).
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- Familial Cancer, 2015, v. 14, n. 1, p. 175, doi. 10.1007/s10689-014-9768-6
- Publication type:
- Article
Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk.
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- Familial Cancer, 2015, v. 14, n. 1, p. 135, doi. 10.1007/s10689-014-9769-5
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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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- Familial Cancer, 2015, v. 14, n. 1, p. 81, doi. 10.1007/s10689-014-9746-z
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- Article