Works matching IS 13899600 AND DT 2013 AND VI 12 AND IP 3
Results: 31
A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis.
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- Familial Cancer, 2013, v. 12, n. 3, p. 573, doi. 10.1007/s10689-012-9587-6
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- Article
Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients.
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- Familial Cancer, 2013, v. 12, n. 3, p. 503, doi. 10.1007/s10689-012-9595-6
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- Article
The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis.
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- Familial Cancer, 2013, v. 12, n. 3, p. 449, doi. 10.1007/s10689-013-9607-1
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- Article
A complex endocrine conundrum.
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- Familial Cancer, 2013, v. 12, n. 3, p. 577, doi. 10.1007/s10689-012-9594-7
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- Article
Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India.
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- Familial Cancer, 2013, v. 12, n. 3, p. 489, doi. 10.1007/s10689-012-9590-y
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- Article
Erratum to: Birt-Hogg-Dubé syndrome: from gene discovery to molecularly targeted therapies.
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- 2013
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- Publication type:
- Correction Notice
Birt-Hogg-Dubé syndrome and the skin.
- Published in:
- Familial Cancer, 2013, v. 12, n. 3, p. 381, doi. 10.1007/s10689-013-9600-8
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- Publication type:
- Article
A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation.
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- Familial Cancer, 2013, v. 12, n. 3, p. 373, doi. 10.1007/s10689-012-9593-8
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- Article
Abstracts.
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- Familial Cancer, 2013, v. 12, n. 3, p. 405, doi. 10.1007/s10689-013-9678-z
- Publication type:
- Article
Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?
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- Familial Cancer, 2013, v. 12, n. 3, p. 563, doi. 10.1007/s10689-012-9597-4
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- Article
Erratum to: Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis.
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- 2013
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- Publication type:
- Correction Notice
Birt-Hogg-Dubé syndrome.
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- Familial Cancer, 2013, v. 12, n. 3, p. 355, doi. 10.1007/s10689-013-9679-y
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- Publication type:
- Article
Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green.
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- Familial Cancer, 2013, v. 12, n. 3, p. 519, doi. 10.1007/s10689-013-9606-2
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- Publication type:
- Article
Splice site mutations in mismatch repair genes and risk of cancer in the general population.
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- Familial Cancer, 2013, v. 12, n. 3, p. 567, doi. 10.1007/s10689-013-9601-7
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- Publication type:
- Article
Erratum to: Closing the loop: an interactive action research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment.
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- 2013
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- Publication type:
- Correction Notice
Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes.
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- Familial Cancer, 2013, v. 12, n. 3, p. 555, doi. 10.1007/s10689-013-9617-z
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- Publication type:
- Article
Erratum to: Birt-Hogg-Dubé: beyond the clinical manifestations.
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- 2013
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- Publication type:
- Correction Notice
Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer.
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- Familial Cancer, 2013, v. 12, n. 3, p. 479, doi. 10.1007/s10689-012-9588-5
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- Publication type:
- Article
Mutation screen and RNA analysis disclose the changed splicing of the E-cadherin transcription in gastric cancer.
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- Familial Cancer, 2013, v. 12, n. 3, p. 547, doi. 10.1007/s10689-013-9619-x
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- Publication type:
- Article
Birt-Hogg-Dubé syndrome: from gene discovery to molecularly targeted therapies.
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- Familial Cancer, 2013, v. 12, n. 3, p. 357, doi. 10.1007/s10689-012-9574-y
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- Publication type:
- Article
Unmet support needs and distress among women with a BRCA1/ 2 mutation.
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- Familial Cancer, 2013, v. 12, n. 3, p. 509, doi. 10.1007/s10689-012-9596-5
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- Publication type:
- Article
Mutation screening in a Norwegian cohort with pheochromocytoma.
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- Familial Cancer, 2013, v. 12, n. 3, p. 529, doi. 10.1007/s10689-013-9608-0
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- Publication type:
- Article
Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial.
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- Familial Cancer, 2013, v. 12, n. 3, p. 537, doi. 10.1007/s10689-013-9609-z
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- Publication type:
- Article
GNAS is not involved in gastrointestinal tumour formation in Peutz-Jeghers syndrome.
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- 2013
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- Publication type:
- Letter
Familial adenomatous polyposis: not all masses are desmoids.
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- Familial Cancer, 2013, v. 12, n. 3, p. 525, doi. 10.1007/s10689-012-9580-0
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- Publication type:
- Article
The risk of gastric cancer in carriers of CHEK2 mutations.
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- Familial Cancer, 2013, v. 12, n. 3, p. 473, doi. 10.1007/s10689-012-9599-2
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- Publication type:
- Article
Birt-Hogg-Dubé: tumour suppressor function and signalling dynamics central to folliculin.
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- Familial Cancer, 2013, v. 12, n. 3, p. 367, doi. 10.1007/s10689-012-9576-9
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- Publication type:
- Article
Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis.
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- Familial Cancer, 2013, v. 12, n. 3, p. 459, doi. 10.1007/s10689-013-9658-3
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- Publication type:
- Article
Cancer family history triage: a key step in the decision to offer screening and genetic testing.
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- Familial Cancer, 2013, v. 12, n. 3, p. 497, doi. 10.1007/s10689-012-9589-4
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- Publication type:
- Article
Pulmonary manifestations of Birt-Hogg-Dubé syndrome.
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- Familial Cancer, 2013, v. 12, n. 3, p. 387, doi. 10.1007/s10689-013-9660-9
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- Publication type:
- Article
Diagnosis and management of BHD-associated kidney cancer.
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- Familial Cancer, 2013, v. 12, n. 3, p. 397, doi. 10.1007/s10689-013-9657-4
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- Publication type:
- Article