| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma
|
Donner, Iikki
|
|
2018
|
18 |
1 |
p. 113-119
|
artikel
|
| 2 |
Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variant
|
Bonis, Maria De
|
|
2018
|
18 |
1 |
p. 29-35
|
artikel
|
| 3 |
Cholesterol profile in women with premature menopause after risk reducing salpingo-oophorectomy
|
Teixeira, Natalia
|
|
2018
|
18 |
1 |
p. 19-27
|
artikel
|
| 4 |
Clinical and pathologic characteristics of breast cancer patients carrying the c.3481_3491del11 mutation
|
El Tannouri, R.
|
|
2018
|
18 |
1 |
p. 1-8
|
artikel
|
| 5 |
Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer
|
Bush, Lisa
|
|
2018
|
18 |
1 |
p. 105-108
|
artikel
|
| 6 |
Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori
|
Hakkaart, Christopher
|
|
2018
|
18 |
1 |
p. 83-90
|
artikel
|
| 7 |
Hemangioblastoma in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome: a phenotypic overlap between VHL and HLRCC Syndromes
|
Dow, Eryn
|
|
2018
|
18 |
1 |
p. 91-95
|
artikel
|
| 8 |
Identification of a novel GREM1 duplication in a patient with multiple colon polyps
|
McKenna, Danielle B.
|
|
2018
|
18 |
1 |
p. 63-66
|
artikel
|
| 9 |
Low-level parental mosaicism in an apparent de novo case of Peutz–Jeghers syndrome
|
Butel-Simoes, G. I.
|
|
2018
|
18 |
1 |
p. 109-112
|
artikel
|
| 10 |
Modified capture–recapture estimates of the number of families with Lynch syndrome in Central Ohio
|
Ranola, John Michael O.
|
|
2018
|
18 |
1 |
p. 67-73
|
artikel
|
| 11 |
Outcome of thyroid ultrasound screening in FAP patients with a normal baseline exam
|
Monachese, Marc
|
|
2018
|
18 |
1 |
p. 75-82
|
artikel
|
| 12 |
Physician interpretation of variants of uncertain significance
|
Macklin, Sarah K.
|
|
2018
|
18 |
1 |
p. 121-126
|
artikel
|
| 13 |
Prevalence of thyroid diseases in familial adenomatous polyposis: a systematic review and meta-analysis
|
Chenbhanich, Jirat
|
|
2018
|
18 |
1 |
p. 53-62
|
artikel
|
| 14 |
Reminders of cancer risk and pain catastrophizing: relationships with cancer worry and perceived risk in women with a first-degree relative with breast cancer
|
Whitney, Colette A.
|
|
2018
|
18 |
1 |
p. 9-18
|
artikel
|
| 15 |
Report of a bi-allelic truncating germline mutation in TP53
|
Brown, Natasha J.
|
|
2018
|
18 |
1 |
p. 101-104
|
artikel
|
| 16 |
Sarcoma in neurofibromatosis 2: case report and review of the literature
|
Linder, C.
|
|
2018
|
18 |
1 |
p. 97-100
|
artikel
|
| 17 |
The BRCA1 exon 13 duplication: clinical characteristics of 22 families in Northern Sweden
|
Edwinsdotter Ardnor, Christina
|
|
2018
|
18 |
1 |
p. 37-42
|
artikel
|
| 18 |
The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study
|
Reumkens, Kelly
|
|
2018
|
18 |
1 |
p. 137-146
|
artikel
|
| 19 |
The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice
|
Menko, Fred H
|
|
2018
|
18 |
1 |
p. 127-135
|
artikel
|
| 20 |
Unsolicited information letters to increase awareness of Lynch syndrome and familial colorectal cancer: reactions and attitudes
|
Petersen, Helle Vendel
|
|
2018
|
18 |
1 |
p. 43-51
|
artikel
|
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