Works matching IS 13899600 AND DT 2010 AND VI 9 AND IP 2
Results: 21
Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation.
- Published in:
- Familial Cancer, 2010, v. 9, n. 2, p. 167, doi. 10.1007/s10689-009-9302-4
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- Article
Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing.
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- Familial Cancer, 2010, v. 9, n. 2, p. 203, doi. 10.1007/s10689-009-9303-3
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- Article
Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing.
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- Familial Cancer, 2010, v. 9, n. 2, p. 187, doi. 10.1007/s10689-009-9301-5
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- Article
Erratum to: FAP-associated desmoid invasiveness correlates with in vitro resistance to doxorubicin.
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- 2010
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- Publication type:
- Correction Notice
Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/ 2 mutation detection.
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- Familial Cancer, 2010, v. 9, n. 2, p. 193, doi. 10.1007/s10689-009-9305-1
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- Article
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome.
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- Familial Cancer, 2010, v. 9, n. 2, p. 245, doi. 10.1007/s10689-009-9312-2
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- Article
Serum antibodies against frameshift peptides in microsatellite unstable colorectal cancer patients with Lynch syndrome.
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- Familial Cancer, 2010, v. 9, n. 2, p. 173, doi. 10.1007/s10689-009-9307-z
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- Article
Evolving perspectives on genetic discrimination in health insurance among health care providers.
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- Familial Cancer, 2010, v. 9, n. 2, p. 253, doi. 10.1007/s10689-009-9308-y
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- Publication type:
- Article
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 years.
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- Familial Cancer, 2010, v. 9, n. 2, p. 213, doi. 10.1007/s10689-009-9311-3
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- Publication type:
- Article
Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient.
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- Familial Cancer, 2010, v. 9, n. 2, p. 239, doi. 10.1007/s10689-009-9306-0
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- Publication type:
- Article
Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis.
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- Familial Cancer, 2010, v. 9, n. 2, p. 99, doi. 10.1007/s10689-009-9290-4
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- Article
An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC.
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- Familial Cancer, 2010, v. 9, n. 2, p. 141, doi. 10.1007/s10689-009-9298-9
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- Publication type:
- Article
Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.
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- Familial Cancer, 2010, v. 9, n. 2, p. 125, doi. 10.1007/s10689-009-9293-1
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- Publication type:
- Article
A PALB2 germline mutation associated with hereditary breast cancer in Italy.
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- Familial Cancer, 2010, v. 9, n. 2, p. 181, doi. 10.1007/s10689-009-9295-z
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- Publication type:
- Article
Mutation analysis of the APC gene in Taiwanese FAP families: low incidence of APC germline mutation in a distinct subgroup of FAP families.
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- Familial Cancer, 2010, v. 9, n. 2, p. 117, doi. 10.1007/s10689-009-9292-2
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- Publication type:
- Article
Outcomes of nasopharyngeal carcinoma screening for high risk family members in Hong Kong.
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- Familial Cancer, 2010, v. 9, n. 2, p. 221, doi. 10.1007/s10689-009-9296-y
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- Publication type:
- Article
Clinical and histomolecular endometrial tumor characterization of patients at-risk for Lynch syndrome in South of Brazil.
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- Familial Cancer, 2010, v. 9, n. 2, p. 131, doi. 10.1007/s10689-009-9297-x
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- Publication type:
- Article
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.
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- Familial Cancer, 2010, v. 9, n. 2, p. 109, doi. 10.1007/s10689-009-9291-3
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- Publication type:
- Article
Heredity, diet and lifestyle as determining risk factors for the esophageal cancer on Nanao Island in Southern China.
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- Familial Cancer, 2010, v. 9, n. 2, p. 229, doi. 10.1007/s10689-009-9300-6
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- Publication type:
- Article
Biallelic MYH germline mutations as cause of Muir-Torre syndrome.
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- Familial Cancer, 2010, v. 9, n. 2, p. 151, doi. 10.1007/s10689-009-9309-x
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- Publication type:
- Article
Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto Rico.
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- Familial Cancer, 2010, v. 9, n. 2, p. 155, doi. 10.1007/s10689-009-9310-4
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- Article