| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abstracts 3rd Biennial Meeting of InSiGHT (International Society for Gastrointestinal Hereditary Tumours)
|
|
|
2010
|
9 |
4 |
p. 713-748
|
artikel
|
| 2 |
A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han
|
Guo, Hong
|
|
2010
|
9 |
4 |
p. 599-603
|
artikel
|
| 3 |
A novel mutation of the Succinate Dehydrogenase B Gene in a Korean Family with Pheochromocytoma
|
Lee, Sang Ah
|
|
2010
|
9 |
4 |
p. 643-646
|
artikel
|
| 4 |
Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations
|
Yang, Xiaohong Rose
|
|
2010
|
9 |
4 |
p. 625-633
|
artikel
|
| 5 |
BRCA1 and BRCA2 families and the risk of skin cancer
|
Ginsburg, Ophira M.
|
|
2010
|
9 |
4 |
p. 489-493
|
artikel
|
| 6 |
BRCA1 mutations and colorectal cancer in Poland
|
Suchy, Janina
|
|
2010
|
9 |
4 |
p. 541-544
|
artikel
|
| 7 |
Breast cancer susceptibility variants alter risk in familial ovarian cancer
|
Latif, A.
|
|
2010
|
9 |
4 |
p. 503-506
|
artikel
|
| 8 |
Can a phenotype for recessive inheritance in breast cancer be defined?
|
Ellberg, Carolina
|
|
2010
|
9 |
4 |
p. 525-530
|
artikel
|
| 9 |
CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland
|
Jakubowska, Anna
|
|
2010
|
9 |
4 |
p. 605-608
|
artikel
|
| 10 |
Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation
|
Gomy, Israel
|
|
2010
|
9 |
4 |
p. 635-642
|
artikel
|
| 11 |
Communicating genetic risk information within families: a review
|
Wiseman, Mel
|
|
2010
|
9 |
4 |
p. 691-703
|
artikel
|
| 12 |
Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population
|
Negura, Lucian
|
|
2010
|
9 |
4 |
p. 519-523
|
artikel
|
| 13 |
Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer
|
Cavallone, Luca
|
|
2010
|
9 |
4 |
p. 507-517
|
artikel
|
| 14 |
Contribution of CDKN2A/P16INK4A, P14ARF, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma
|
Buecher, B.
|
|
2010
|
9 |
4 |
p. 663-667
|
artikel
|
| 15 |
Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives
|
Hayat Roshanai, Afsaneh
|
|
2010
|
9 |
4 |
p. 669-679
|
artikel
|
| 16 |
FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review
|
Lynch, Henry T.
|
|
2010
|
9 |
4 |
p. 581-588
|
artikel
|
| 17 |
Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry
|
Silva, Felipe Carneiro da
|
|
2010
|
9 |
4 |
p. 563-570
|
artikel
|
| 18 |
Hereditary predisposition rather than environmental factor are likely to explain the familial link between uveal melanoma and other cancers
|
Abdel-Rahman, M. H.
|
|
2010
|
9 |
4 |
p. 661-662
|
artikel
|
| 19 |
Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation
|
Lim, Eu Jin
|
|
2010
|
9 |
4 |
p. 555-561
|
artikel
|
| 20 |
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions
|
Lefevre, Jérémie H.
|
|
2010
|
9 |
4 |
p. 589-594
|
artikel
|
| 21 |
PALB2: a novel inactivating mutation in a Italian breast cancer family
|
Balia, Cristina
|
|
2010
|
9 |
4 |
p. 531-536
|
artikel
|
| 22 |
Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning
|
Maheu, Christine
|
|
2010
|
9 |
4 |
p. 617-624
|
artikel
|
| 23 |
Papillary thyroid cancer in a patient with MUTYH-associated polyposis (MAP)
|
Pervaiz, Muhammad Ali
|
|
2010
|
9 |
4 |
p. 595-597
|
artikel
|
| 24 |
Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality
|
You, Y. Nancy
|
|
2010
|
9 |
4 |
p. 609-616
|
artikel
|
| 25 |
Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of PENN II model to previous study
|
Lindor, Noralane M.
|
|
2010
|
9 |
4 |
p. 495-502
|
artikel
|
| 26 |
Real world experience with cancer genetic counseling via telephone
|
Sutphen, Rebecca
|
|
2010
|
9 |
4 |
p. 681-689
|
artikel
|
| 27 |
Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits
|
Lammens, C. R. M.
|
|
2010
|
9 |
4 |
p. 647-654
|
artikel
|
| 28 |
Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009
|
Kohonen-Corish, Maija
|
|
2010
|
9 |
4 |
p. 705-711
|
artikel
|
| 29 |
Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families
|
Solyom, Szilvia
|
|
2010
|
9 |
4 |
p. 537-540
|
artikel
|
| 30 |
Selective COX-2 inhibition affects fatty acids, but not COX mRNA expression in patients with FAP
|
Almendingen, Kari
|
|
2010
|
9 |
4 |
p. 571-580
|
artikel
|
| 31 |
Similarities in solar ultraviolet irradiance and other environmental factors may explain much of the family link between uveal melanoma and other cancers
|
Grant, William B.
|
|
2010
|
9 |
4 |
p. 659-660
|
artikel
|
| 32 |
The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers
|
Vargas, Ana Cristina
|
|
2010
|
9 |
4 |
p. 545-553
|
artikel
|
| 33 |
Thymoma associated with malignancies may herald a hereditary cancer syndrome
|
Tehrani, Omid Saeed
|
|
2010
|
9 |
4 |
p. 655-657
|
artikel
|
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