Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             25 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis? Johannesma, Paul C.
2015
15 2 p. 297-300
artikel
2 Associations between allergic conditions and pediatric brain tumors in Neurofibromatosis type 1 Porcelli, Bree
2015
15 2 p. 301-308
artikel
3 CDH1 germline mutations and hereditary lobular breast cancer Corso, Giovanni
2016
15 2 p. 215-219
artikel
4 Constitutional MLH1 methylation presenting with colonic polyposis syndrome and not Lynch syndrome Kidambi, Trilokesh D.
2016
15 2 p. 275-280
artikel
5 Correlation between the germline methylation status in ERβ promoter and the risk in prostate cancer: a prospective study Wang, Lihui
2015
15 2 p. 309-315
artikel
6 CYP1A1 and GSTP1 gene variations in breast cancer: a systematic review and case–control study Akhtar, Sumaira
2015
15 2 p. 201-214
artikel
7 Determining the familial risk distribution of colorectal cancer: a data mining approach Chau, Rowena
2015
15 2 p. 241-251
artikel
8 Developing and assessing the utility of a You-Tube based clinical genetics video channel for families affected by inherited tumours Jones, G. E.
2016
15 2 p. 351-355
artikel
9 Development of a novel PTT assay for mutation detection in PALB2 large exons and PALB2 screening in medullary breast cancer Poumpouridou, Nikoleta
2015
15 2 p. 183-191
artikel
10 Diagnostic values of osteopontin combined with CA125 for ovarian cancer: a meta-analysis Lan, Zhu
2015
15 2 p. 221-230
artikel
11 Erratum to: Methylation of the miR-126 gene associated with glioma progression Cui, Hongwei
2015
15 2 p. 325
artikel
12 Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis Spier, Isabel
2016
15 2 p. 281-288
artikel
13 Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer Douma, Kirsten F. L.
2015
15 2 p. 231-240
artikel
14 Germline BAP1 mutations misreported as somatic based on tumor-only testing Abdel-Rahman, Mohamed H.
2016
15 2 p. 327-330
artikel
15 Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment Baumgart, Leigh A.
2015
15 2 p. 331-339
artikel
16 Methylation of the miR-126 gene associated with glioma progression Cui, Hongwei
2015
15 2 p. 317-324
artikel
17 Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study Baars, J. E.
2016
15 2 p. 163-171
artikel
18 Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis Haraldsdottir, Sigurdis
2015
15 2 p. 253-260
artikel
19 Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients Taki, Keiko
2015
15 2 p. 261-265
artikel
20 Non-genetic health professionals’ attitude towards, knowledge of and skills in discussing and ordering genetic testing for hereditary cancer Douma, Kirsten F. L.
2015
15 2 p. 341-350
artikel
21 Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect Vogelaar, Ingrid P.
2015
15 2 p. 289-296
artikel
22 Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer Murria Estal, Rosa
2015
15 2 p. 193-200
artikel
23 Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis Casellas-Cabrera, Nicolás
2015
15 2 p. 267-274
artikel
24 Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis Oliveira, Eneida Santos de
2015
15 2 p. 173-181
artikel
25 The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety Sermijn, Erica
2016
15 2 p. 155-162
artikel
                             25 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland