Works matching IS 13899600 AND DT 2016 AND VI 15 AND IP 2
Results: 25
Diagnostic values of osteopontin combined with CA125 for ovarian cancer: a meta-analysis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 221, doi. 10.1007/s10689-015-9847-3
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- Publication type:
- Article
Erratum to: Methylation of the miR-126 gene associated with glioma progression.
- Published in:
- 2016
- By:
- Publication type:
- Erratum
CYP1A1 and GSTP1 gene variations in breast cancer: a systematic review and case-control study.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 201, doi. 10.1007/s10689-015-9849-1
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- Publication type:
- Article
Correlation between the germline methylation status in ERβ promoter and the risk in prostate cancer: a prospective study.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 309, doi. 10.1007/s10689-015-9850-8
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- Publication type:
- Article
Development of a novel PTT assay for mutation detection in PALB2 large exons and PALB2 screening in medullary breast cancer.
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- Familial Cancer, 2016, v. 15, n. 2, p. 183, doi. 10.1007/s10689-015-9851-7
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- Publication type:
- Article
Non-genetic health professionals' attitude towards, knowledge of and skills in discussing and ordering genetic testing for hereditary cancer.
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- Familial Cancer, 2016, v. 15, n. 2, p. 341, doi. 10.1007/s10689-015-9852-6
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- Publication type:
- Article
Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 297, doi. 10.1007/s10689-015-9853-5
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- Publication type:
- Article
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.
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- Familial Cancer, 2016, v. 15, n. 2, p. 155, doi. 10.1007/s10689-015-9854-4
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- Publication type:
- Article
Associations between allergic conditions and pediatric brain tumors in Neurofibromatosis type 1.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 301, doi. 10.1007/s10689-015-9855-3
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- Publication type:
- Article
Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis.
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- Familial Cancer, 2016, v. 15, n. 2, p. 253, doi. 10.1007/s10689-015-9856-2
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- Publication type:
- Article
Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients.
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- Familial Cancer, 2016, v. 15, n. 2, p. 261, doi. 10.1007/s10689-015-9857-1
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- Publication type:
- Article
Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 173, doi. 10.1007/s10689-015-9858-0
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- Publication type:
- Article
Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 289, doi. 10.1007/s10689-015-9859-z
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- Publication type:
- Article
Determining the familial risk distribution of colorectal cancer: a data mining approach.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 241, doi. 10.1007/s10689-015-9860-6
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- Publication type:
- Article
Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 231, doi. 10.1007/s10689-015-9861-5
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- Publication type:
- Article
Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 267, doi. 10.1007/s10689-015-9862-4
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- Publication type:
- Article
Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 331, doi. 10.1007/s10689-015-9863-3
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- Publication type:
- Article
Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 193, doi. 10.1007/s10689-015-9864-2
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- Publication type:
- Article
Germline BAP1 mutations misreported as somatic based on tumor-only testing.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 327, doi. 10.1007/s10689-016-9865-9
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- Publication type:
- Article
Developing and assessing the utility of a You-Tube based clinical genetics video channel for families affected by inherited tumours.
- Published in:
- 2016
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- Publication type:
- Letter
Constitutional MLH1 methylation presenting with colonic polyposis syndrome and not Lynch syndrome.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 275, doi. 10.1007/s10689-016-9868-6
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- Publication type:
- Article
CDH1 germline mutations and hereditary lobular breast cancer.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 215, doi. 10.1007/s10689-016-9869-5
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- Publication type:
- Article
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 281, doi. 10.1007/s10689-016-9870-z
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- Publication type:
- Article
Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 163, doi. 10.1007/s10689-016-9871-y
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- Publication type:
- Article
Methylation of the miR-126 gene associated with glioma progression.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 317, doi. 10.1007/s10689-015-9846-4
- By:
- Publication type:
- Article