Works matching IS 13899600 AND DT 2012 AND VI 11 AND IP 4
Results: 22
Hope-based intervention for individuals susceptible to colorectal cancer: a pilot study.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 545, doi. 10.1007/s10689-012-9545-3
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- Publication type:
- Article
Advanced duodenal disease in familial adenomatous polyposis: how frequently should patients be followed up after successful therapy?
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 553, doi. 10.1007/s10689-012-9546-2
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- Publication type:
- Article
Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 559, doi. 10.1007/s10689-012-9547-1
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- Publication type:
- Article
Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 571, doi. 10.1007/s10689-012-9550-6
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- Publication type:
- Article
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomas.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 653, doi. 10.1007/s10689-012-9549-z
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- Publication type:
- Article
Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 565, doi. 10.1007/s10689-012-9548-0
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- Publication type:
- Article
Portuguese c.156_157insAlu BRCA2 founder mutation: gastrointestinal and tongue neoplasias may be part of the phenotype.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 657, doi. 10.1007/s10689-012-9551-5
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- Publication type:
- Article
Novel mutations of OGG1 base excision repair pathway gene in laryngeal cancer patients.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 587, doi. 10.1007/s10689-012-9554-2
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- Publication type:
- Article
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 661, doi. 10.1007/s10689-012-9553-3
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- Publication type:
- Article
Routine TP53 testing for breast cancer under age 30: ready for prime time?
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 607, doi. 10.1007/s10689-012-9557-z
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- Publication type:
- Article
Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment.
- Published in:
- 2012
- By:
- Publication type:
- Letter
High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 623, doi. 10.1007/s10689-012-9560-4
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- Publication type:
- Article
No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathways.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 601, doi. 10.1007/s10689-012-9556-0
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- Publication type:
- Article
Non-synonymous polymorphism (Gln261Arg) of 12-lipoxygenase in colorectal and thyroid cancers.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 615, doi. 10.1007/s10689-012-9559-x
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- Publication type:
- Article
Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 579, doi. 10.1007/s10689-012-9552-4
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- Publication type:
- Article
Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 595, doi. 10.1007/s10689-012-9555-1
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- Publication type:
- Article
Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 667, doi. 10.1007/s10689-012-9561-3
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- Publication type:
- Article
Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?
- Published in:
- 2012
- By:
- Publication type:
- Letter
Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 637, doi. 10.1007/s10689-012-9564-0
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- Publication type:
- Article
Low penetrance alleles as risk modifiers in familial and sporadic breast cancer.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 629, doi. 10.1007/s10689-012-9563-1
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- Publication type:
- Article
Familial breast cancer: less emotional distress in adult daughters if they provide emotional support to their affected mother.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 645, doi. 10.1007/s10689-012-9566-y
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- Publication type:
- Article
Ovarian metastases of colorectal and duodenal cancer in familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2012, v. 11, n. 4, p. 671, doi. 10.1007/s10689-012-9565-z
- By:
- Publication type:
- Article