Works matching IS 13899600 AND DT 2010 AND VI 9 AND IP 3
Results: 33
Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.
- Published in:
- Familial Cancer, 2010, v. 9, n. 3, p. 283, doi. 10.1007/s10689-010-9345-6
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- Publication type:
- Article
Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome.
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- Familial Cancer, 2010, v. 9, n. 3, p. 345, doi. 10.1007/s10689-009-9314-0
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- Article
Pregnancy after prophylactic total gastrectomy.
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- Familial Cancer, 2010, v. 9, n. 3, p. 331, doi. 10.1007/s10689-009-9316-y
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- Article
Update multiple endocrine neoplasia type 2.
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- Familial Cancer, 2010, v. 9, n. 3, p. 449, doi. 10.1007/s10689-010-9320-2
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- Article
High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome.
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- Familial Cancer, 2010, v. 9, n. 3, p. 383, doi. 10.1007/s10689-010-9321-1
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- Article
“ I have always believed I was at high risk...” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments.
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- Familial Cancer, 2010, v. 9, n. 3, p. 469, doi. 10.1007/s10689-010-9324-y
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- Article
Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients.
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- Familial Cancer, 2010, v. 9, n. 3, p. 443, doi. 10.1007/s10689-010-9323-z
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- Publication type:
- Article
Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study.
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- Familial Cancer, 2010, v. 9, n. 3, p. 305, doi. 10.1007/s10689-010-9325-x
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- Publication type:
- Article
Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel.
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- Familial Cancer, 2010, v. 9, n. 3, p. 327, doi. 10.1007/s10689-010-9337-6
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- Publication type:
- Article
Assessment of clinical practices among cancer genetic counselors.
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- Familial Cancer, 2010, v. 9, n. 3, p. 459, doi. 10.1007/s10689-010-9326-9
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- Publication type:
- Article
RASSF1A polymorphism in familial breast cancer.
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- Familial Cancer, 2010, v. 9, n. 3, p. 263, doi. 10.1007/s10689-010-9335-8
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- Publication type:
- Article
Analysis of mismatch repair gene mutations in Turkish HNPCC patients.
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- Familial Cancer, 2010, v. 9, n. 3, p. 365, doi. 10.1007/s10689-010-9336-7
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- Publication type:
- Article
Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma.
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- Familial Cancer, 2010, v. 9, n. 3, p. 377, doi. 10.1007/s10689-010-9339-4
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- Publication type:
- Article
Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.
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- Familial Cancer, 2010, v. 9, n. 3, p. 267, doi. 10.1007/s10689-010-9338-5
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- Publication type:
- Article
Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence.
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- Familial Cancer, 2010, v. 9, n. 3, p. 291, doi. 10.1007/s10689-010-9327-8
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- Publication type:
- Article
Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain.
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- Familial Cancer, 2010, v. 9, n. 3, p. 297, doi. 10.1007/s10689-009-9313-1
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- Publication type:
- Article
A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype.
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- Familial Cancer, 2010, v. 9, n. 3, p. 395, doi. 10.1007/s10689-009-9317-x
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- Publication type:
- Article
Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family.
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- Familial Cancer, 2010, v. 9, n. 3, p. 275, doi. 10.1007/s10689-009-9315-z
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- Publication type:
- Article
LOH analysis should not be used as a tool to assess whether UVs of BRCA1/2 are pathogenic or not.
- Published in:
- 2010
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- Publication type:
- Letter
A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma.
- Published in:
- Familial Cancer, 2010, v. 9, n. 3, p. 425, doi. 10.1007/s10689-009-9319-8
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- Publication type:
- Article
Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma.
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- Familial Cancer, 2010, v. 9, n. 3, p. 431, doi. 10.1007/s10689-010-9328-7
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- Publication type:
- Article
Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families.
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- Familial Cancer, 2010, v. 9, n. 3, p. 335, doi. 10.1007/s10689-010-9329-6
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- Publication type:
- Article
Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis.
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- Familial Cancer, 2010, v. 9, n. 3, p. 401, doi. 10.1007/s10689-010-9331-z
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- Publication type:
- Article
Location in the large bowel influences the APC mutations observed in FAP adenomas.
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- Familial Cancer, 2010, v. 9, n. 3, p. 389, doi. 10.1007/s10689-010-9332-y
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- Publication type:
- Article
Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers.
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- Familial Cancer, 2010, v. 9, n. 3, p. 313, doi. 10.1007/s10689-010-9333-x
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- Publication type:
- Article
Erratum to: Survey of familial glioma and role of germline p16<sup> INK4A</sup>/ p14<sup> ARF</sup> and p53 mutation.
- Published in:
- 2010
- By:
- Publication type:
- Correction Notice
Survey of familial glioma and role of germline p16<sup> INK4A</sup> /p14<sup> ARF</sup> and p53 mutation.
- Published in:
- Familial Cancer, 2010, v. 9, n. 3, p. 413, doi. 10.1007/s10689-010-9346-5
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- Publication type:
- Article
Screening for germline DND1 mutations in testicular cancer patients.
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- Familial Cancer, 2010, v. 9, n. 3, p. 439, doi. 10.1007/s10689-010-9340-y
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- Publication type:
- Article
Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP?
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- Familial Cancer, 2010, v. 9, n. 3, p. 405, doi. 10.1007/s10689-010-9341-x
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- Publication type:
- Article
Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter?
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- Familial Cancer, 2010, v. 9, n. 3, p. 407, doi. 10.1007/s10689-010-9342-9
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- Publication type:
- Article
Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes.
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- Familial Cancer, 2010, v. 9, n. 3, p. 479, doi. 10.1007/s10689-010-9343-8
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- Publication type:
- Article
Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters.
- Published in:
- Familial Cancer, 2010, v. 9, n. 3, p. 357, doi. 10.1007/s10689-010-9334-9
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- Publication type:
- Article
Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer.
- Published in:
- Familial Cancer, 2010, v. 9, n. 3, p. 321, doi. 10.1007/s10689-010-9344-7
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- Publication type:
- Article