| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier
|
Alanee, Shaheen
|
|
2012
|
12 |
1 |
p. 125-127
|
artikel
|
| 2 |
A novel missense mutation (N78D) in a family with von Hippel–Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts
|
Cingoz, S.
|
|
2012
|
12 |
1 |
p. 111-117
|
artikel
|
| 3 |
An unusual BRCA mutation distribution in a high risk cancer genetics clinic
|
Nelson-Moseke, Anna C.
|
|
2012
|
12 |
1 |
p. 83-87
|
artikel
|
| 4 |
Birt–Hogg–Dubé: beyond the clinical manifestations
|
Middelton, Lindsay A.
|
|
2012
|
12 |
1 |
p. 97-99
|
artikel
|
| 5 |
Catalysts to withdrawal from familial ovarian cancer screening for surgery and reactions to discontinued screening: a qualitative study
|
Lifford, Kate J.
|
|
2012
|
12 |
1 |
p. 19-26
|
artikel
|
| 6 |
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review
|
Knopperts, A. P.
|
|
2012
|
12 |
1 |
p. 43-50
|
artikel
|
| 7 |
Feasibility evaluation of an online tool to guide decisions for BRCA1/2 mutation carriers
|
Schackmann, Elizabeth A.
|
|
2012
|
12 |
1 |
p. 65-73
|
artikel
|
| 8 |
Multiple small “imaging” branch-duct type intraductal papillary mucinous neoplasms (IPMNs) in familial pancreatic cancer: indicator for concomitant high grade pancreatic intraepithelial neoplasia?
|
Bartsch, D. K.
|
|
2012
|
12 |
1 |
p. 89-96
|
artikel
|
| 9 |
Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families
|
Schwarzová, Lucie
|
|
2012
|
12 |
1 |
p. 35-42
|
artikel
|
| 10 |
Prospective enteroscopic evaluation of jejunal polyposis in patients with familial adenomatous polyposis and advanced duodenal polyposis
|
Alderlieste, Y. A.
|
|
2012
|
12 |
1 |
p. 51-56
|
artikel
|
| 11 |
Psychosocial factors and uptake of risk-reducing salpingo-oophorectomy in women at high risk for ovarian cancer
|
Meiser, Bettina
|
|
2012
|
12 |
1 |
p. 101-109
|
artikel
|
| 12 |
10 rare tumors that warrant a genetics referral
|
Banks, Kimberly C.
|
|
2012
|
12 |
1 |
p. 1-18
|
artikel
|
| 13 |
Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors
|
Sourrouille, Isabelle
|
|
2012
|
12 |
1 |
p. 27-33
|
artikel
|
| 14 |
The deletion of exons 3–5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish families
|
Palanca, Sarai
|
|
2012
|
12 |
1 |
p. 119-123
|
artikel
|
| 15 |
The Fourth Birt–Hogg–Dubé Symposium, Cincinnati, USA, 28th–30th March, 2012
|
|
|
2012
|
12 |
1 |
p. 133-140
|
artikel
|
| 16 |
The Fourth Birt–Hogg–Dubé Symposium, Cincinnati, USA, 28th–30th March, 2012
|
|
|
|
12 |
1 |
p. 133-140
|
artikel
|
| 17 |
The prevalence of BRCA mutations among familial breast cancer patients in Korea: results of the Korean Hereditary Breast Cancer study
|
Han, Sang-Ah
|
|
2012
|
12 |
1 |
p. 75-81
|
artikel
|
| 18 |
The spectrum of urological malignancy in Lynch syndrome
|
Barrow, P. J.
|
|
2012
|
12 |
1 |
p. 57-63
|
artikel
|
| 19 |
Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation
|
Kuligina, Ekatherina Sh.
|
|
2012
|
12 |
1 |
p. 129-132
|
artikel
|
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