Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 1
Results: 22
A single visit multidisciplinary model for managing patients with mutations in moderate and high-risk genes in a community practice setting.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 175, doi. 10.1007/s10689-017-0010-1
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- Publication type:
- Article
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 141, doi. 10.1007/s10689-017-0011-0
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- Publication type:
- Article
Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testing.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 87, doi. 10.1007/s10689-017-0012-z
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- Publication type:
- Article
Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 91, doi. 10.1007/s10689-017-0013-y
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- Publication type:
- Article
Development of a high risk pancreatic screening clinic using 3.0 T MRI.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 101, doi. 10.1007/s10689-017-0057-z
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- Publication type:
- Article
Next generation sequencing is informing phenotype: a TP53 example.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 123, doi. 10.1007/s10689-017-0002-1
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- Publication type:
- Article
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 63, doi. 10.1007/s10689-017-0003-0
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- Publication type:
- Article
A multi-gene panel study in hereditary breast and ovarian cancer in Colombia.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 23, doi. 10.1007/s10689-017-0004-z
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- Publication type:
- Article
Association of genetic variations in RTN4 3′-UTR with risk for clear cell renal cell carcinoma.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 129, doi. 10.1007/s10689-017-0005-y
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- Publication type:
- Article
Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 31, doi. 10.1007/s10689-017-0014-x
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- Publication type:
- Article
Contiguous gene deletion of chromosome 2p16.3-p21 as a cause of Lynch syndrome.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 71, doi. 10.1007/s10689-017-0006-x
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- Publication type:
- Article
The importance of a well-structured pancreatic screening program for familial and hereditary pancreatic cancer.
- Published in:
- 2018
- By:
- Publication type:
- Editorial
The role of screening MRI in the era of next generation sequencing and moderate-risk genetic mutations.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 167, doi. 10.1007/s10689-017-0007-9
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- Publication type:
- Article
Early onset renal cell carcinoma in an adolescent girl with germline FLCN exon 5 deletion.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 135, doi. 10.1007/s10689-017-0008-8
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- Publication type:
- Article
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 79, doi. 10.1007/s10689-017-0009-7
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- Publication type:
- Article
How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 155, doi. 10.1007/s10689-017-9994-9
- By:
- Publication type:
- Article
The association of low penetrance genetic risk modifiers with colorectal cancer in lynch syndrome patients: a systematic review and meta-analysis.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 43, doi. 10.1007/s10689-017-9995-8
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- Publication type:
- Article
Quality of life following prophylactic gynecological surgery: experiences of female Lynch mutation carriers.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 53, doi. 10.1007/s10689-017-9997-6
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- Publication type:
- Article
TP53 germline and somatic mutations in a patient with fibrolamellar hepatocellular carcinoma.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 119, doi. 10.1007/s10689-017-9998-5
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- Publication type:
- Article
Is there a genetic anticipation in breast and/or ovarian cancer families with the germline c.3481_3491del11 mutation?
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 5, doi. 10.1007/s10689-017-9999-4
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- Publication type:
- Article
Heightened perception of breast cancer risk in young women at risk of familial breast cancer.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 15, doi. 10.1007/s10689-017-0001-2
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- Publication type:
- Article
Gestational choriocarcinoma associated with a germline TP53 mutation.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 113, doi. 10.1007/s10689-017-9996-7
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- Publication type:
- Article