Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 3
Results: 23
Attitudes and compliance of clinical management after genetic testing for hereditary breast and ovarian cancer among high-risk Southern Chinese females with breast cancer history.
- Published in:
- Familial Cancer, 2014, v. 13, n. 3, p. 423, doi. 10.1007/s10689-014-9706-7
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- Article
Duplex value of caveolin-1 in non-small cell lung cancer: a meta analysis.
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- Familial Cancer, 2014, v. 13, n. 3, p. 449, doi. 10.1007/s10689-014-9707-6
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- Article
Novel BRCA1 deleterious mutation (c.1918C>T) in familial breast and ovarian cancer syndrome who share a common ancestry.
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- Familial Cancer, 2014, v. 13, n. 3, p. 431, doi. 10.1007/s10689-014-9708-5
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- Article
Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome.
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- Familial Cancer, 2014, v. 13, n. 3, p. 459, doi. 10.1007/s10689-014-9709-4
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- Article
Analysis of patient reports on the referral process to two NSW cancer genetic services.
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- Familial Cancer, 2014, v. 13, n. 3, p. 333, doi. 10.1007/s10689-014-9710-y
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- Article
A family history questionnaire improves detection of women at risk for hereditary gynecologic cancer: a pilot study.
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- Familial Cancer, 2014, v. 13, n. 3, p. 469, doi. 10.1007/s10689-014-9711-x
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- Article
Intronic splicing mutations in PTCH1 cause Gorlin syndrome.
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- Familial Cancer, 2014, v. 13, n. 3, p. 477, doi. 10.1007/s10689-014-9712-9
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- Article
Two Chinese pedigrees for adenomatous polyposis coli: new mutations at codon 1309 and predisposition to phenotypic variations.
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- Familial Cancer, 2014, v. 13, n. 3, p. 361, doi. 10.1007/s10689-014-9713-8
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- Article
Fertility and apparent genetic anticipation in Lynch syndrome.
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- Familial Cancer, 2014, v. 13, n. 3, p. 369, doi. 10.1007/s10689-014-9714-7
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- Article
Influence of family history on psychosocial distress and perceived need for treatment in prostate cancer survivors.
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- Familial Cancer, 2014, v. 13, n. 3, p. 481, doi. 10.1007/s10689-014-9715-6
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- Article
Erratum to: Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India.
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- 2014
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- Publication type:
- Erratum
BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan.
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- Familial Cancer, 2014, v. 13, n. 3, p. 437, doi. 10.1007/s10689-014-9717-4
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- Article
An unusual case of familial adenomatous polyposis with very early symptom occurrence.
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- Familial Cancer, 2014, v. 13, n. 3, p. 375, doi. 10.1007/s10689-014-9718-3
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- Article
A survey of the practice patterns of gynecologic oncologists dealing with hereditary cancer patients in Japan.
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- Familial Cancer, 2014, v. 13, n. 3, p. 489, doi. 10.1007/s10689-014-9719-2
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- Article
Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.
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- Familial Cancer, 2014, v. 13, n. 3, p. 381, doi. 10.1007/s10689-014-9720-9
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- Article
BRCA1 founder mutations compared to ovarian cancer in Belarus.
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- Familial Cancer, 2014, v. 13, n. 3, p. 445, doi. 10.1007/s10689-014-9721-8
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- Article
Genetics of endometrial cancer.
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- Familial Cancer, 2014, v. 13, n. 3, p. 499, doi. 10.1007/s10689-014-9722-7
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- Article
'Would you test your children without their consent?' and other sticky dilemmas in the field of cancer genetic testing.
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- Familial Cancer, 2014, v. 13, n. 3, p. 345, doi. 10.1007/s10689-014-9723-6
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- Publication type:
- Article
How harmful is genetic testing for familial adenomatous polyposis (FAP) in young children; the parents' experience.
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- Familial Cancer, 2014, v. 13, n. 3, p. 391, doi. 10.1007/s10689-014-9724-5
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- Article
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.
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- Familial Cancer, 2014, v. 13, n. 3, p. 507, doi. 10.1007/s10689-014-9725-4
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- Article
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns.
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- Familial Cancer, 2014, v. 13, n. 3, p. 401, doi. 10.1007/s10689-014-9726-3
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- Article
Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate.
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- Familial Cancer, 2014, v. 13, n. 3, p. 415, doi. 10.1007/s10689-014-9727-2
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- Article
Limited diagnostic value of microsatellite instability associated pathology features in colorectal cancer.
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- Familial Cancer, 2014, v. 13, n. 3, p. 351, doi. 10.1007/s10689-014-9705-8
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- Article