| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome
|
Takahashi, Masanobu
|
|
2012
|
11 |
4 |
p. 559-564
|
artikel
|
| 2 |
Advanced duodenal disease in familial adenomatous polyposis: how frequently should patients be followed up after successful therapy?
|
Balmforth, Damian C.
|
|
2012
|
11 |
4 |
p. 553-557
|
artikel
|
| 3 |
Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome
|
Serrano, Miguel
|
|
2012
|
11 |
4 |
p. 571-578
|
artikel
|
| 4 |
Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation
|
Therkildsen, Christina
|
|
2012
|
11 |
4 |
p. 579-585
|
artikel
|
| 5 |
Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act
|
Allain, Dawn C.
|
|
2012
|
11 |
4 |
p. 637-644
|
artikel
|
| 6 |
Familial breast cancer: less emotional distress in adult daughters if they provide emotional support to their affected mother
|
Vodermaier, Andrea
|
|
2012
|
11 |
4 |
p. 645-652
|
artikel
|
| 7 |
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma
|
Smetsers, Stephanie
|
|
2012
|
11 |
4 |
p. 661-665
|
artikel
|
| 8 |
High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer
|
Gaj, Pawel
|
|
2012
|
11 |
4 |
p. 623-628
|
artikel
|
| 9 |
Hope-based intervention for individuals susceptible to colorectal cancer: a pilot study
|
Ho, Samuel Mun-yin
|
|
2012
|
11 |
4 |
p. 545-551
|
artikel
|
| 10 |
Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer
|
Zuhlke, Kimberly A.
|
|
2012
|
11 |
4 |
p. 595-600
|
artikel
|
| 11 |
Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?
|
Grandval, Philippe
|
|
2012
|
11 |
4 |
p. 681-683
|
artikel
|
| 12 |
Low penetrance alleles as risk modifiers in familial and sporadic breast cancer
|
Esteban Cardeñosa, Eva
|
|
2012
|
11 |
4 |
p. 629-636
|
artikel
|
| 13 |
Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations
|
Lindor, Noralane M.
|
|
2012
|
11 |
4 |
p. 667-669
|
artikel
|
| 14 |
No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathways
|
Penkert, Judith
|
|
2012
|
11 |
4 |
p. 601-606
|
artikel
|
| 15 |
Non-synonymous polymorphism (Gln261Arg) of 12-lipoxygenase in colorectal and thyroid cancers
|
Prasad, Vidudala V. T. S.
|
|
2012
|
11 |
4 |
p. 615-621
|
artikel
|
| 16 |
Novel mutations of OGG1 base excision repair pathway gene in laryngeal cancer patients
|
Mahjabeen, Ishrat
|
|
2012
|
11 |
4 |
p. 587-593
|
artikel
|
| 17 |
Ovarian metastases of colorectal and duodenal cancer in familial adenomatous polyposis
|
Crobach, Stijn
|
|
2012
|
11 |
4 |
p. 671-673
|
artikel
|
| 18 |
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomas
|
Johnson, K. J.
|
|
2012
|
11 |
4 |
p. 653-656
|
artikel
|
| 19 |
Portuguese c.156_157insAlu BRCA2 founder mutation: gastrointestinal and tongue neoplasias may be part of the phenotype
|
Moreira, Miguel A. M.
|
|
2012
|
11 |
4 |
p. 657-660
|
artikel
|
| 20 |
Routine TP53 testing for breast cancer under age 30: ready for prime time?
|
McCuaig, Jeanna M.
|
|
2012
|
11 |
4 |
p. 607-613
|
artikel
|
| 21 |
Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment
|
Belvederesi, Laura
|
|
2012
|
11 |
4 |
p. 675-680
|
artikel
|
| 22 |
Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation
|
Kijima, Chihiro
|
|
2012
|
11 |
4 |
p. 565-570
|
artikel
|
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