| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A family history questionnaire improves detection of women at risk for hereditary gynecologic cancer: a pilot study
|
Koeneman, Margot M.
|
|
2014
|
13 |
3 |
p. 469-475
|
artikel
|
| 2 |
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns
|
Borelli, Iolanda
|
|
2014
|
13 |
3 |
p. 401-413
|
artikel
|
| 3 |
Analysis of patient reports on the referral process to two NSW cancer genetic services
|
Butel-Simoes, Grace I.
|
|
2014
|
13 |
3 |
p. 333-343
|
artikel
|
| 4 |
An unusual case of familial adenomatous polyposis with very early symptom occurrence
|
Ponz de Leon, Maurizio
|
|
2014
|
13 |
3 |
p. 375-380
|
artikel
|
| 5 |
A survey of the practice patterns of gynecologic oncologists dealing with hereditary cancer patients in Japan
|
Tanabe, Noriko
|
|
2014
|
13 |
3 |
p. 489-498
|
artikel
|
| 6 |
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
|
Kwong, Ava
|
|
2014
|
13 |
3 |
p. 423-430
|
artikel
|
| 7 |
BRCA1 founder mutations compared to ovarian cancer in Belarus
|
Savanevich, Alena
|
|
2014
|
13 |
3 |
p. 445-447
|
artikel
|
| 8 |
BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan
|
Biunno, Ida
|
|
2014
|
13 |
3 |
p. 437-444
|
artikel
|
| 9 |
Duplex value of caveolin-1 in non-small cell lung cancer: a meta analysis
|
Chen, Dali
|
|
2014
|
13 |
3 |
p. 449-457
|
artikel
|
| 10 |
Erratum to: Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India
|
Chakraborty, Abhijit
|
|
2014
|
13 |
3 |
p. 513
|
artikel
|
| 11 |
Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives
|
Dilzell, Kristen
|
|
2014
|
13 |
3 |
p. 381-389
|
artikel
|
| 12 |
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies
|
Renella, R.
|
|
2014
|
13 |
3 |
p. 507-511
|
artikel
|
| 13 |
Fertility and apparent genetic anticipation in Lynch syndrome
|
Stupart, Douglas
|
|
2014
|
13 |
3 |
p. 369-374
|
artikel
|
| 14 |
Genetics of endometrial cancer
|
Shai, Ayelet
|
|
2014
|
13 |
3 |
p. 499-505
|
artikel
|
| 15 |
How harmful is genetic testing for familial adenomatous polyposis (FAP) in young children; the parents’ experience
|
Kattentidt-Mouravieva, Anna A.
|
|
2014
|
13 |
3 |
p. 391-399
|
artikel
|
| 16 |
Influence of family history on psychosocial distress and perceived need for treatment in prostate cancer survivors
|
Dinkel, Andreas
|
|
2014
|
13 |
3 |
p. 481-488
|
artikel
|
| 17 |
Intronic splicing mutations in PTCH1 cause Gorlin syndrome
|
Bholah, Zaynab
|
|
2014
|
13 |
3 |
p. 477-480
|
artikel
|
| 18 |
Limited diagnostic value of microsatellite instability associated pathology features in colorectal cancer
|
Putten, Paul G. van
|
|
2014
|
13 |
3 |
p. 351-359
|
artikel
|
| 19 |
Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome
|
Salo-Mullen, Erin E.
|
|
2014
|
13 |
3 |
p. 459-467
|
artikel
|
| 20 |
Novel BRCA1 deleterious mutation (c.1918C>T) in familial breast and ovarian cancer syndrome who share a common ancestry
|
Gabaldó Barrios, Xavier
|
|
2014
|
13 |
3 |
p. 431-435
|
artikel
|
| 21 |
Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate
|
Hozyasz, Kamil K.
|
|
2014
|
13 |
3 |
p. 415-421
|
artikel
|
| 22 |
Two Chinese pedigrees for adenomatous polyposis coli: new mutations at codon 1309 and predisposition to phenotypic variations
|
Liao, Dai-Xiang
|
|
2014
|
13 |
3 |
p. 361-368
|
artikel
|
| 23 |
“Would you test your children without their consent?” and other sticky dilemmas in the field of cancer genetic testing
|
Brierley, Karina L.
|
|
2014
|
13 |
3 |
p. 345-350
|
artikel
|
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