Works matching IS 13899600 AND DT 2016 AND VI 15 AND IP 4
Results: 25
Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies.
- Published in:
- Familial Cancer, 2016, v. 15, n. 4, p. 553, doi. 10.1007/s10689-016-9872-x
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- Publication type:
- Article
Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis.
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- Familial Cancer, 2016, v. 15, n. 4, p. 497, doi. 10.1007/s10689-016-9873-9
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- Article
A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma.
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- Familial Cancer, 2016, v. 15, n. 4, p. 601, doi. 10.1007/s10689-016-9874-8
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- Article
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.
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- Familial Cancer, 2016, v. 15, n. 4, p. 507, doi. 10.1007/s10689-016-9875-7
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- Article
Modeling the dyadic effects of parenting, stress, and coping on parent-child communication in families tested for hereditary breast-ovarian cancer risk.
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- Familial Cancer, 2016, v. 15, n. 4, p. 513, doi. 10.1007/s10689-016-9876-6
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- Article
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.
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- Familial Cancer, 2016, v. 15, n. 4, p. 563, doi. 10.1007/s10689-016-9877-5
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- Article
Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma.
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- Familial Cancer, 2016, v. 15, n. 4, p. 607, doi. 10.1007/s10689-016-9879-3
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- Article
Evaluation of laboratory perspectives on hereditary cancer panels.
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- Familial Cancer, 2016, v. 15, n. 4, p. 689, doi. 10.1007/s10689-016-9880-x
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- Publication type:
- Article
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study.
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- Familial Cancer, 2016, v. 15, n. 4, p. 697, doi. 10.1007/s10689-016-9889-1
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- Article
Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India.
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- Familial Cancer, 2016, v. 15, n. 4, p. 617, doi. 10.1007/s10689-016-9891-7
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- Publication type:
- Article
MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics.
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- Familial Cancer, 2016, v. 15, n. 4, p. 625, doi. 10.1007/s10689-016-9892-6
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- Publication type:
- Article
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation.
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- Familial Cancer, 2016, v. 15, n. 4, p. 571, doi. 10.1007/s10689-016-9894-4
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- Publication type:
- Article
Evaluation of TP53 Pro72Arg and MDM2 SNP285-SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations.
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- Familial Cancer, 2016, v. 15, n. 4, p. 635, doi. 10.1007/s10689-016-9895-3
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- Publication type:
- Article
No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families.
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- Familial Cancer, 2016, v. 15, n. 4, p. 523, doi. 10.1007/s10689-016-9898-0
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- Publication type:
- Article
An investigation of the factors effecting high-risk individuals' decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC).
- Published in:
- Familial Cancer, 2016, v. 15, n. 4, p. 665, doi. 10.1007/s10689-016-9910-8
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- Publication type:
- Article
CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome.
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- Familial Cancer, 2016, v. 15, n. 4, p. 579, doi. 10.1007/s10689-016-9899-z
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- Publication type:
- Article
Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency.
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- Familial Cancer, 2016, v. 15, n. 4, p. 587, doi. 10.1007/s10689-016-9902-8
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- Publication type:
- Article
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome.
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- Familial Cancer, 2016, v. 15, n. 4, p. 645, doi. 10.1007/s10689-016-9906-4
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- Publication type:
- Article
Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families.
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- Familial Cancer, 2016, v. 15, n. 4, p. 651, doi. 10.1007/s10689-016-9907-3
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- Publication type:
- Article
Angelina and Brad effect.
- Published in:
- 2016
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- Publication type:
- Letter
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer.
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- Familial Cancer, 2016, v. 15, n. 4, p. 529, doi. 10.1007/s10689-016-9900-x
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- Publication type:
- Article
Occurrence of renal cell carcinoma and hematologic malignancies (predominantly lymphoid) in individuals and in families.
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- Familial Cancer, 2016, v. 15, n. 4, p. 677, doi. 10.1007/s10689-016-9911-7
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- Publication type:
- Article
A model for patient-direct screening and referral for familial cancer risk.
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- Familial Cancer, 2016, v. 15, n. 4, p. 707, doi. 10.1007/s10689-016-9912-6
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- Publication type:
- Article
Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes.
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- Familial Cancer, 2016, v. 15, n. 4, p. 593, doi. 10.1007/s10689-016-9914-4
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- Publication type:
- Article
Decentralized colonoscopic surveillance with high patient compliance prevents hereditary and familial colorectal cancer.
- Published in:
- Familial Cancer, 2016, v. 15, n. 4, p. 543, doi. 10.1007/s10689-016-9867-7
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- Publication type:
- Article