Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 4
Results: 18
Genetic 135G/C polymorphism of RAD51 gene and risk of cancer: a meta-analysis of 28,956 cases and 28,372 controls.
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- Familial Cancer, 2014, v. 13, n. 4, p. 515, doi. 10.1007/s10689-014-9729-0
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Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samples.
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- Familial Cancer, 2014, v. 13, n. 4, p. 583, doi. 10.1007/s10689-014-9730-7
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Association of interleukin-23 receptor gene polymorphisms with risk of bladder cancer in Chinese.
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- Familial Cancer, 2014, v. 13, n. 4, p. 619, doi. 10.1007/s10689-014-9731-6
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Cribriform-morular variant of papillary thyroid carcinoma: an indication to screen for occult FAP.
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- Familial Cancer, 2014, v. 13, n. 4, p. 547, doi. 10.1007/s10689-014-9732-5
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- Article
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients.
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- Familial Cancer, 2014, v. 13, n. 4, p. 553, doi. 10.1007/s10689-014-9733-4
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- Article
'It's all very well reading the letters in the genome, but it's a long way to being able to write': Men's interpretations of undergoing genetic profiling to determine future risk of prostate cancer.
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- Familial Cancer, 2014, v. 13, n. 4, p. 625, doi. 10.1007/s10689-014-9734-3
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Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment.
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- Familial Cancer, 2014, v. 13, n. 4, p. 637, doi. 10.1007/s10689-014-9735-2
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Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.
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- Familial Cancer, 2014, v. 13, n. 4, p. 645, doi. 10.1007/s10689-014-9736-1
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A primary care audit of familial risk in patients with a personal history of breast cancer.
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- Familial Cancer, 2014, v. 13, n. 4, p. 591, doi. 10.1007/s10689-014-9737-0
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- Article
Phenotype of SDHB mutation carriers in the Netherlands.
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- Familial Cancer, 2014, v. 13, n. 4, p. 651, doi. 10.1007/s10689-014-9738-z
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A polymorphism at miRNA-122-binding site in the IL-1α 3′UTR is associated with risk of epithelial ovarian cancer.
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- Familial Cancer, 2014, v. 13, n. 4, p. 595, doi. 10.1007/s10689-014-9739-y
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- Article
High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families.
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- Familial Cancer, 2014, v. 13, n. 4, p. 603, doi. 10.1007/s10689-014-9740-5
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- Article
Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice.
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- Familial Cancer, 2014, v. 13, n. 4, p. 527, doi. 10.1007/s10689-014-9741-4
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- Article
The secondary bile acid, deoxycholate accelerates intestinal adenoma-adenocarcinoma sequence in Apc mice through enhancing Wnt signaling.
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- Familial Cancer, 2014, v. 13, n. 4, p. 563, doi. 10.1007/s10689-014-9742-3
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Molecular heterogeneity of familial myeloproliferative neoplasms revealed by analysis of the commonly acquired JAK2, CALR and MPL mutations.
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- Familial Cancer, 2014, v. 13, n. 4, p. 659, doi. 10.1007/s10689-014-9743-2
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Association of reduced XRCC2 expression with lymph node metastasis in breast cancer tissues.
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- Familial Cancer, 2014, v. 13, n. 4, p. 611, doi. 10.1007/s10689-014-9745-0
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- Article
Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.
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- Familial Cancer, 2014, v. 13, n. 4, p. 537, doi. 10.1007/s10689-014-9728-1
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- Article
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry.
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- Familial Cancer, 2014, v. 13, n. 4, p. 573, doi. 10.1007/s10689-014-9744-1
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- Article