| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro)
|
Vale Rodrigues, Rita
|
|
2016
|
16 |
2 |
p. 267-270
|
artikel
|
| 2 |
All in the family? Analyzing the impact of family history in addition to genotype on medullary thyroid carcinoma aggressiveness in MEN2A patients
|
Long, Kristin L.
|
|
2016
|
16 |
2 |
p. 283-289
|
artikel
|
| 3 |
Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe
|
Bogdanova, Natalia
|
|
2016
|
16 |
2 |
p. 181-186
|
artikel
|
| 4 |
Attenuated polyposis of the large bowel: a morphologic and molecular approach
|
Leon, Maurizio Ponz de
|
|
2016
|
16 |
2 |
p. 211-220
|
artikel
|
| 5 |
BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer
|
Jamard, Estelle
|
|
2016
|
16 |
2 |
p. 167-171
|
artikel
|
| 6 |
Cancer screening behaviors and risk perceptions among family members of colorectal cancer patients with unexplained mismatch repair deficiency
|
Katz, Lior H.
|
|
2016
|
16 |
2 |
p. 231-237
|
artikel
|
| 7 |
Colonoscopy in Lynch syndrome: the need for a new quality score
|
Boonstra, Jurjen J.
|
|
2016
|
16 |
2 |
p. 239-241
|
artikel
|
| 8 |
Cystic parathyroid glands in MEN1: A rare entity?
|
Cavalli, Tiziana
|
|
2016
|
16 |
2 |
p. 249-256
|
artikel
|
| 9 |
DICER1 mutation and tumors associated with a familial tumor predisposition syndrome: practical considerations
|
Bardón-Cancho, Eduardo J.
|
|
2016
|
16 |
2 |
p. 291-294
|
artikel
|
| 10 |
Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumor
|
Goehringer, Caroline
|
|
2016
|
16 |
2 |
p. 303-309
|
artikel
|
| 11 |
Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer
|
Nilsson, Martin P.
|
|
2017
|
16 |
2 |
p. 187-193
|
artikel
|
| 12 |
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
|
Rohlin, Anna
|
|
2016
|
16 |
2 |
p. 195-203
|
artikel
|
| 13 |
Four generations of SDHB-related disease: complexities in management
|
Srirangalingam, U.
|
|
2016
|
16 |
2 |
p. 279-282
|
artikel
|
| 14 |
Pain evaluation during gynaecological surveillance in women with Lynch syndrome
|
Helder-Woolderink, Jorien
|
|
2016
|
16 |
2 |
p. 205-210
|
artikel
|
| 15 |
Recurrent TP53 missense mutation in cancer patients of Arab descent
|
Zick, Aviad
|
|
2016
|
16 |
2 |
p. 295-301
|
artikel
|
| 16 |
Risk algorithms that include pathology adjustment for HER2 amplification need to make further downward adjustments in likelihood scores
|
Evans, D. G.
|
|
2016
|
16 |
2 |
p. 173-179
|
artikel
|
| 17 |
TP53 and CDKN1A mutation analysis in families with Li–Fraumeni and Li–Fraumeni like syndromes
|
Andrade, Raissa Coelho
|
|
2016
|
16 |
2 |
p. 243-248
|
artikel
|
| 18 |
Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome
|
Wielders, Eva
|
|
2016
|
16 |
2 |
p. 221-229
|
artikel
|
| 19 |
Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma (CDKN2A) in Norway
|
Levin, Trine
|
|
2016
|
16 |
2 |
p. 257-265
|
artikel
|
| 20 |
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands
|
Dommering, Charlotte J.
|
|
2016
|
16 |
2 |
p. 271-277
|
artikel
|
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