Works matching IS 13899600 AND DT 2011 AND VI 10 AND IP 2
Results: 30
Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition.
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- Familial Cancer, 2011, v. 10, n. 2, p. 319, doi. 10.1007/s10689-010-9401-2
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- Article
Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma.
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- Familial Cancer, 2011, v. 10, n. 2, p. 355, doi. 10.1007/s10689-010-9402-1
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The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer.
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- Familial Cancer, 2011, v. 10, n. 2, p. 331, doi. 10.1007/s10689-010-9403-0
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- Article
IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer.
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- Familial Cancer, 2011, v. 10, n. 2, p. 173, doi. 10.1007/s10689-010-9404-z
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- Article
Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.
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- Familial Cancer, 2011, v. 10, n. 2, p. 239, doi. 10.1007/s10689-010-9406-x
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- Article
Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report.
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- Familial Cancer, 2011, v. 10, n. 2, p. 255, doi. 10.1007/s10689-010-9409-7
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The impact of cancer pathology confirmation on clinical management of a family history of cancer.
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- Familial Cancer, 2011, v. 10, n. 2, p. 373, doi. 10.1007/s10689-010-9407-9
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Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma.
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- Familial Cancer, 2011, v. 10, n. 2, p. 315, doi. 10.1007/s10689-010-9405-y
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- Article
Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).
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- Familial Cancer, 2011, v. 10, n. 2, p. 245, doi. 10.1007/s10689-010-9408-8
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- Article
Familial gastric cancer: update for practice management.
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- Familial Cancer, 2011, v. 10, n. 2, p. 391, doi. 10.1007/s10689-010-9410-1
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A new frameshift MEN1 gene mutation associated with familial malignant insulinomas.
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- Familial Cancer, 2011, v. 10, n. 2, p. 343, doi. 10.1007/s10689-010-9412-z
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Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.
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- Familial Cancer, 2011, v. 10, n. 2, p. 337, doi. 10.1007/s10689-010-9411-0
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- Article
Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish family.
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- Familial Cancer, 2011, v. 10, n. 2, p. 349, doi. 10.1007/s10689-010-9413-y
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- Article
German national case collection for familial pancreatic cancer (FaPaCa): ten years experience.
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- Familial Cancer, 2011, v. 10, n. 2, p. 323, doi. 10.1007/s10689-010-9414-x
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- Article
Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome.
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- Familial Cancer, 2011, v. 10, n. 2, p. 265, doi. 10.1007/s10689-010-9416-8
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Early occurrence of lung adenocarcinoma and breast cancer after radiotherapy of a chest wall sarcoma in a patient with a de novo germline mutation in TP53.
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- Familial Cancer, 2011, v. 10, n. 2, p. 187, doi. 10.1007/s10689-010-9415-9
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Impact of computer-assisted data collection, evaluation and management on the cancer genetic counselor's time providing patient care.
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- Familial Cancer, 2011, v. 10, n. 2, p. 381, doi. 10.1007/s10689-011-9417-2
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- Article
A clinical perspective on genetic counseling and testing during end of life care for women with recurrent progressive ovarian cancer: opportunities and challenges.
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- Familial Cancer, 2011, v. 10, n. 2, p. 193, doi. 10.1007/s10689-011-9418-1
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Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation.
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- Familial Cancer, 2011, v. 10, n. 2, p. 285, doi. 10.1007/s10689-011-9419-0
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Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations.
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- Familial Cancer, 2011, v. 10, n. 2, p. 207, doi. 10.1007/s10689-011-9422-5
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Novel germline SDHD mutation: diagnosis and implications to the patient.
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- Familial Cancer, 2011, v. 10, n. 2, p. 365, doi. 10.1007/s10689-011-9421-6
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Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study.
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- Familial Cancer, 2011, v. 10, n. 2, p. 199, doi. 10.1007/s10689-011-9420-7
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Clinical characteristics and outcomes in familial adenomatous polyposis patients with a long-term treatment of celecoxib: a matched cohort study.
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- Familial Cancer, 2011, v. 10, n. 2, p. 303, doi. 10.1007/s10689-011-9423-4
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Mutation deep within an intron of MSH2 causes Lynch syndrome.
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- Familial Cancer, 2011, v. 10, n. 2, p. 297, doi. 10.1007/s10689-011-9427-0
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PALB2 mutations in familial breast and pancreatic cancer.
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- Familial Cancer, 2011, v. 10, n. 2, p. 225, doi. 10.1007/s10689-011-9426-1
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BRCA1/2 genetic testing uptake and psychosocial outcomes in men.
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- Familial Cancer, 2011, v. 10, n. 2, p. 213, doi. 10.1007/s10689-011-9425-2
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A new phenotypic manifestation of familial adenomatous polyposis.
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- Familial Cancer, 2011, v. 10, n. 2, p. 309, doi. 10.1007/s10689-011-9432-3
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A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer.
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- Familial Cancer, 2011, v. 10, n. 2, p. 233, doi. 10.1007/s10689-011-9429-y
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Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics.
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- Familial Cancer, 2011, v. 10, n. 2, p. 397, doi. 10.1007/s10689-011-9428-z
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Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies.
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- Familial Cancer, 2011, v. 10, n. 2, p. 273, doi. 10.1007/s10689-011-9431-4
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