| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A clinical perspective on genetic counseling and testing during end of life care for women with recurrent progressive ovarian cancer: opportunities and challenges
|
Daniels, Molly S.
|
|
2011
|
10 |
2 |
p. 193-197
|
artikel
|
| 2 |
Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome
|
Medina-Arana, V.
|
|
2011
|
10 |
2 |
p. 265-271
|
artikel
|
| 3 |
A new frameshift MEN1 gene mutation associated with familial malignant insulinomas
|
Hasani-Ranjbar, Shirin
|
|
2010
|
10 |
2 |
p. 343-348
|
artikel
|
| 4 |
A new phenotypic manifestation of familial adenomatous polyposis
|
Edelstein, Daniel L.
|
|
2011
|
10 |
2 |
p. 309-313
|
artikel
|
| 5 |
A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer
|
Kwong, Ava
|
|
2011
|
10 |
2 |
p. 233-237
|
artikel
|
| 6 |
BRCA1/2 genetic testing uptake and psychosocial outcomes in men
|
Graves, Kristi D.
|
|
2011
|
10 |
2 |
p. 213-223
|
artikel
|
| 7 |
Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish family
|
McKay, L.
|
|
2010
|
10 |
2 |
p. 349-353
|
artikel
|
| 8 |
Clinical characteristics and outcomes in familial adenomatous polyposis patients with a long-term treatment of celecoxib: a matched cohort study
|
Huang, Kui
|
|
2011
|
10 |
2 |
p. 303-308
|
artikel
|
| 9 |
Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer
|
Isinger-Ekstrand, Anna
|
|
2010
|
10 |
2 |
p. 239-243
|
artikel
|
| 10 |
Early occurrence of lung adenocarcinoma and breast cancer after radiotherapy of a chest wall sarcoma in a patient with a de novo germline mutation in TP53
|
Ferrarini, Alessandra
|
|
2011
|
10 |
2 |
p. 187-192
|
artikel
|
| 11 |
Familial gastric cancer: update for practice management
|
Corso, Giovanni
|
|
2010
|
10 |
2 |
p. 391-396
|
artikel
|
| 12 |
Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study
|
Yoon, Sook-Yee
|
|
2011
|
10 |
2 |
p. 199-205
|
artikel
|
| 13 |
German national case collection for familial pancreatic cancer (FaPaCa): ten years experience
|
Schneider, Ralph
|
|
2011
|
10 |
2 |
p. 323-330
|
artikel
|
| 14 |
Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics
|
Lehtonen, Heli J.
|
|
2011
|
10 |
2 |
p. 397-411
|
artikel
|
| 15 |
Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics
|
Lehtonen, Heli J.
|
|
|
10 |
2 |
p. 397-411
|
artikel
|
| 16 |
Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma
|
Slade, Ingrid
|
|
2010
|
10 |
2 |
p. 337-342
|
artikel
|
| 17 |
Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation
|
Lastella, Patrizia
|
|
2011
|
10 |
2 |
p. 285-295
|
artikel
|
| 18 |
IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer
|
Henningson, Maria
|
|
2010
|
10 |
2 |
p. 173-185
|
artikel
|
| 19 |
Impact of computer-assisted data collection, evaluation and management on the cancer genetic counselor’s time providing patient care
|
Cohen, Stephanie A.
|
|
2011
|
10 |
2 |
p. 381-389
|
artikel
|
| 20 |
Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition
|
Abdel-Rahman, Mohamed H.
|
|
2010
|
10 |
2 |
p. 319-321
|
artikel
|
| 21 |
Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
|
Roberts, Aedan
|
|
2010
|
10 |
2 |
p. 245-254
|
artikel
|
| 22 |
Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies
|
Hardt, Karin
|
|
2011
|
10 |
2 |
p. 273-284
|
artikel
|
| 23 |
Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma
|
Sabbaghian, N.
|
|
2010
|
10 |
2 |
p. 315-317
|
artikel
|
| 24 |
Mutation deep within an intron of MSH2 causes Lynch syndrome
|
Clendenning, Mark
|
|
2011
|
10 |
2 |
p. 297-301
|
artikel
|
| 25 |
Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report
|
Vogelsang, Matjaz
|
|
2010
|
10 |
2 |
p. 255-263
|
artikel
|
| 26 |
Novel germline SDHD mutation: diagnosis and implications to the patient
|
Varghese, Jeena
|
|
2011
|
10 |
2 |
p. 365-371
|
artikel
|
| 27 |
PALB2 mutations in familial breast and pancreatic cancer
|
Hofstatter, Erin W.
|
|
2011
|
10 |
2 |
p. 225-231
|
artikel
|
| 28 |
Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma
|
Hensen, Erik F.
|
|
2010
|
10 |
2 |
p. 355-363
|
artikel
|
| 29 |
Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations
|
Hansen, Thomas v. O.
|
|
2011
|
10 |
2 |
p. 207-212
|
artikel
|
| 30 |
The impact of cancer pathology confirmation on clinical management of a family history of cancer
|
Edwards, E.
|
|
2010
|
10 |
2 |
p. 373-380
|
artikel
|
| 31 |
The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer
|
Li, Ning
|
|
2010
|
10 |
2 |
p. 331-336
|
artikel
|
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