Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 2
Results: 20
Discovery of mutations in homologous recombination genes in African-American women with breast cancer.
- Published in:
- Familial Cancer, 2018, v. 17, n. 2, p. 187, doi. 10.1007/s10689-017-0036-4
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- Article
Dental anomalies in pediatric patients with familial adenomatous polyposis.
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- Familial Cancer, 2018, v. 17, n. 2, p. 229, doi. 10.1007/s10689-017-0035-5
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- Article
Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in <italic>TP53</italic> germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic.
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- Familial Cancer, 2018, v. 17, n. 2, p. 287, doi. 10.1007/s10689-017-0034-6
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- Article
Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing.
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- Familial Cancer, 2018, v. 17, n. 2, p. 309, doi. 10.1007/s10689-017-0033-7
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- Article
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic <italic>MSH2</italic> somatic mutations.
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- Familial Cancer, 2018, v. 17, n. 2, p. 281, doi. 10.1007/s10689-017-0032-8
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- Article
Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent <italic>MLH1</italic> hypermethylation and <italic>MSH2</italic> somatic mutations.
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- Familial Cancer, 2018, v. 17, n. 2, p. 225, doi. 10.1007/s10689-017-0031-9
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- Article
A germline missense mutation in exon 3 of the <italic>MSH2</italic> gene in a Lynch syndrome family: correlation with phenotype and localization assay.
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- Familial Cancer, 2018, v. 17, n. 2, p. 215, doi. 10.1007/s10689-017-0030-x
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- Article
Pancreatic neuroendocrine tumor in a patient with a <italic>TSC1</italic> variant: case report and review of the literature.
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- Familial Cancer, 2018, v. 17, n. 2, p. 275, doi. 10.1007/s10689-017-0029-3
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- Article
p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in <italic>TP53</italic> R337H mutation carriers.
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- Familial Cancer, 2018, v. 17, n. 2, p. 269, doi. 10.1007/s10689-017-0028-4
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- Article
Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan.
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- Familial Cancer, 2018, v. 17, n. 2, p. 261, doi. 10.1007/s10689-017-0027-5
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- Article
Pancreatic adenocarcinoma with a germline <italic>PTEN</italic> p.Arg234Gln mutation.
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- Familial Cancer, 2018, v. 17, n. 2, p. 255, doi. 10.1007/s10689-017-0025-7
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- Article
Remarkable effects of imatinib in a family with young onset gastrointestinal stromal tumors and cutaneous hyperpigmentation associated with a germline <italic>KIT</italic>-Trp557Arg mutation: case report and literature overview.
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- Familial Cancer, 2018, v. 17, n. 2, p. 247, doi. 10.1007/s10689-017-0024-8
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- Article
Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families.
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- Familial Cancer, 2018, v. 17, n. 2, p. 213, doi. 10.1007/s10689-017-0023-9
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- Article
Novel <italic>BRCA1</italic> splice-site mutation in ovarian cancer patients of Slavic origin.
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- Familial Cancer, 2018, v. 17, n. 2, p. 179, doi. 10.1007/s10689-017-0022-x
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- Article
Issues related to family history of cancer at the end of life: a palliative care providers’ survey.
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- Familial Cancer, 2018, v. 17, n. 2, p. 303, doi. 10.1007/s10689-017-0021-y
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- Article
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
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- Familial Cancer, 2018, v. 17, n. 2, p. 235, doi. 10.1007/s10689-017-0019-5
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- Publication type:
- Article
A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families.
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- Familial Cancer, 2018, v. 17, n. 2, p. 209, doi. 10.1007/s10689-017-0018-6
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- Article
A comparison of cosegregation analysis methods for the clinical setting.
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- Familial Cancer, 2018, v. 17, n. 2, p. 295, doi. 10.1007/s10689-017-0017-7
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- Article
Screening of <italic>BMPR1a</italic> for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.
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- Familial Cancer, 2018, v. 17, n. 2, p. 205, doi. 10.1007/s10689-017-0016-8
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- Article
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing.
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- Familial Cancer, 2018, v. 17, n. 2, p. 197, doi. 10.1007/s10689-017-0015-9
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- Article