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41 results found

no	title	author	magazine	year	volume	issue	page(s)	type
1	A high frequent BRCA1 founder mutation identified in the Greenlandic population	Harboe, Theresa Larriba		2009	8	4	p. 413-419	article
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	article
3	Are prediction models for Lynch syndrome valid for probands with endometrial cancer?	Backes, Floor J.		2009	8	4	p. 483-487	article
4	Association of MUTYH and MSH6 germline mutations in colorectal cancer patients	Giráldez, María Dolores		2009	8	4	p. 525-531	article
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	article
6	Attitude towards pre-implantation genetic diagnosis for hereditary cancer	Lammens, Chantal		2009	8	4	p. 457-464	article
7	Cancer genetic predisposition: information needs of patients irrespective of risk level	Metcalfe, Alison		2009	8	4	p. 403-412	article
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	article
9	Cancer risk in a cohort of subjects carrying a single mismatch repair gene mutation	Stupart, D. A.		2009	8	4	p. 519-523	article
10	Characterization of the largest kindred with MEN2A due to a Cys609Ser RET mutation	Mian, Caterina		2009	8	4	p. 379-382	article
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	article
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	article
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	article
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	article
15	FAP-associated desmoid invasiveness correlates with in vitro resistance to doxorubicin	Joyner, David E.		2009	8	4	p. 569-580	article
16	First case report of Muir–Torre syndrome associated with non-small cell lung cancer	Nolan, L.		2009	8	4	p. 359-362	article
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	article
18	Genetic polymorphism in ornithine decarboxylase and risk of breast cancer	Brown, Iain		2009	8	4	p. 307-311	article
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	article
20	Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome	Gargiulo, S.		2009	8	4	p. 547-553	article
21	Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations	Kaufman, Bella		2009	8	4	p. 473-478	article
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	article
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	article
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	article
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	article
26	Methylation not a frequent “second hit” in tumors with germline BRCA mutations	Dworkin, Amy M.		2009	8	4	p. 339-346	article
27	Molecular study of CEPBA in familial hematological malignancies	Abed, R. El		2009	8	4	p. 581-584	article
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	article
29	PALB2 sequence variants in young South African breast cancer patients	Sluiter, Michelle		2009	8	4	p. 347-353	article
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	article
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	article
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	article
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	article
34	Strategies for endometrial screening in the Lynch syndrome population: a patient acceptability study	Elmasry, K.		2009	8	4	p. 431-439	article
35	Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals	McKinnon, Wendy		2009	8	4	p. 363-369	article
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	article
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	article
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	article
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	article
40	TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset	Pinto, Carla		2009	8	4	p. 383-390	article
41	Younger age-at-diagnosis for familial malignant testicular germ cell tumor	Mai, Phuong L.		2009	8	4	p. 451-456	article

41 results found

Koninklijke Bibliotheek - National Library of the Netherlands