| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A high frequent BRCA1 founder mutation identified in the Greenlandic population
|
Harboe, Theresa Larriba
|
|
2009
|
8 |
4 |
p. 413-419
|
artikel
|
| 2 |
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis
|
Walsh, Michael D.
|
|
2009
|
8 |
4 |
p. 313-323
|
artikel
|
| 3 |
Are prediction models for Lynch syndrome valid for probands with endometrial cancer?
|
Backes, Floor J.
|
|
2009
|
8 |
4 |
p. 483-487
|
artikel
|
| 4 |
Association of MUTYH and MSH6 germline mutations in colorectal cancer patients
|
Giráldez, María Dolores
|
|
2009
|
8 |
4 |
p. 525-531
|
artikel
|
| 5 |
A study on MSH2 and MLH1 mutations in hereditary nonpolyposis colorectal cancer families from the Basque Country, describing four new germline mutations
|
Martínez-Bouzas, Cristina
|
|
2009
|
8 |
4 |
p. 533-539
|
artikel
|
| 6 |
Attitude towards pre-implantation genetic diagnosis for hereditary cancer
|
Lammens, Chantal
|
|
2009
|
8 |
4 |
p. 457-464
|
artikel
|
| 7 |
Cancer genetic predisposition: information needs of patients irrespective of risk level
|
Metcalfe, Alison
|
|
2009
|
8 |
4 |
p. 403-412
|
artikel
|
| 8 |
Cancer prevention and screening practices among women at risk for hereditary breast and ovarian cancer after genetic counseling in the community setting
|
Morgan, Debra
|
|
2009
|
8 |
4 |
p. 277-287
|
artikel
|
| 9 |
Cancer risk in a cohort of subjects carrying a single mismatch repair gene mutation
|
Stupart, D. A.
|
|
2009
|
8 |
4 |
p. 519-523
|
artikel
|
| 10 |
Characterization of the largest kindred with MEN2A due to a Cys609Ser RET mutation
|
Mian, Caterina
|
|
2009
|
8 |
4 |
p. 379-382
|
artikel
|
| 11 |
CHEK2*1100delC does not contribute to risk to breast cancer among Malay, Chinese and Indians in Malaysia
|
Thirthagiri, Eswary
|
|
2009
|
8 |
4 |
p. 355-358
|
artikel
|
| 12 |
Conflict between values and technology: perceptions of preimplantation genetic diagnosis among women at increased risk for hereditary breast and ovarian cancer
|
Quinn, Gwendolyn P.
|
|
2009
|
8 |
4 |
p. 441-449
|
artikel
|
| 13 |
Determination of splice-site mutations in Lynch syndrome (hereditary non-polyposis colorectal cancer) patients using functional splicing assay
|
Naruse, Hiromu
|
|
2009
|
8 |
4 |
p. 509-517
|
artikel
|
| 14 |
Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for lynch syndrome
|
Zighelboim, Israel
|
|
2009
|
8 |
4 |
p. 501-504
|
artikel
|
| 15 |
FAP-associated desmoid invasiveness correlates with in vitro resistance to doxorubicin
|
Joyner, David E.
|
|
2009
|
8 |
4 |
p. 569-580
|
artikel
|
| 16 |
First case report of Muir–Torre syndrome associated with non-small cell lung cancer
|
Nolan, L.
|
|
2009
|
8 |
4 |
p. 359-362
|
artikel
|
| 17 |
Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients
|
Christensen, Lise Lotte
|
|
2009
|
8 |
4 |
p. 489-500
|
artikel
|
| 18 |
Genetic polymorphism in ornithine decarboxylase and risk of breast cancer
|
Brown, Iain
|
|
2009
|
8 |
4 |
p. 307-311
|
artikel
|
| 19 |
Genetic testing for Lynch syndrome in the first year of colorectal cancer: a review of the psychological impact
|
Landsbergen, Karin M.
|
|
2009
|
8 |
4 |
p. 325-337
|
artikel
|
| 20 |
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome
|
Gargiulo, S.
|
|
2009
|
8 |
4 |
p. 547-553
|
artikel
|
| 21 |
Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations
|
Kaufman, Bella
|
|
2009
|
8 |
4 |
p. 473-478
|
artikel
|
| 22 |
Identification of a de novo BRCA1 mutation in a woman with early onset bilateral breast cancer
|
Edwards, Emma
|
|
2009
|
8 |
4 |
p. 479-482
|
artikel
|
| 23 |
Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing
|
Marafie, Makia J.
|
|
2009
|
8 |
4 |
p. 289-298
|
artikel
|
| 24 |
Improvement of endometrial biopsy over transvaginal ultrasound alone for endometrial surveillance in women with Lynch syndrome
|
Gerritzen, Lotte H. M.
|
|
2009
|
8 |
4 |
p. 391-397
|
artikel
|
| 25 |
Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population
|
Seong, Moon-Woo
|
|
2009
|
8 |
4 |
p. 505-508
|
artikel
|
| 26 |
Methylation not a frequent “second hit” in tumors with germline BRCA mutations
|
Dworkin, Amy M.
|
|
2009
|
8 |
4 |
p. 339-346
|
artikel
|
| 27 |
Molecular study of CEPBA in familial hematological malignancies
|
Abed, R. El
|
|
2009
|
8 |
4 |
p. 581-584
|
artikel
|
| 28 |
Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease
|
Hasani-Ranjbar, Shirin
|
|
2009
|
8 |
4 |
p. 465-471
|
artikel
|
| 29 |
PALB2 sequence variants in young South African breast cancer patients
|
Sluiter, Michelle
|
|
2009
|
8 |
4 |
p. 347-353
|
artikel
|
| 30 |
Patient preferences and National Health Service costs: a cost-consequences analysis of cancer genetic services
|
Griffith, Gethin L.
|
|
2008
|
8 |
4 |
p. 265-275
|
artikel
|
| 31 |
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes
|
Chaudru, Valérie
|
|
2009
|
8 |
4 |
p. 371-377
|
artikel
|
| 32 |
p53 tetramerization domain mutations: germline R342X and R342P, and somatic R337G identified in pediatric patients with Li–Fraumeni syndrome and a child with adrenocortical carcinoma
|
Fiszer-Maliszewska, Lucja
|
|
2009
|
8 |
4 |
p. 541-546
|
artikel
|
| 33 |
Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome
|
Berginc, Gašper
|
|
2009
|
8 |
4 |
p. 421-429
|
artikel
|
| 34 |
Strategies for endometrial screening in the Lynch syndrome population: a patient acceptability study
|
Elmasry, K.
|
|
2009
|
8 |
4 |
p. 431-439
|
artikel
|
| 35 |
Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals
|
McKinnon, Wendy
|
|
2009
|
8 |
4 |
p. 363-369
|
artikel
|
| 36 |
The correlation between a family history of colorectal cancer and survival of patients with colorectal cancer
|
Birgisson, Helgi
|
|
2009
|
8 |
4 |
p. 555-561
|
artikel
|
| 37 |
The prevalence of germ-line TP53 mutations in women diagnosed with breast cancer before age 30
|
Ginsburg, Ophira M.
|
|
2009
|
8 |
4 |
p. 563-567
|
artikel
|
| 38 |
The relationship between knowledge of family history and cancer characteristics at diagnosis in women newly-diagnosed with invasive breast cancer
|
Lijovic, Marijana
|
|
2009
|
8 |
4 |
p. 299-305
|
artikel
|
| 39 |
The RNF146 and ECHDC1 genes as candidates for inherited breast and ovarian cancer in Jewish Ashkenazi women
|
Menachem, Tal Distelman
|
|
2009
|
8 |
4 |
p. 399-402
|
artikel
|
| 40 |
TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset
|
Pinto, Carla
|
|
2009
|
8 |
4 |
p. 383-390
|
artikel
|
| 41 |
Younger age-at-diagnosis for familial malignant testicular germ cell tumor
|
Mai, Phuong L.
|
|
2009
|
8 |
4 |
p. 451-456
|
artikel
|
Tijdschrift beschrijving