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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A comparison of cosegregation analysis methods for the clinical setting Rañola, John Michael O.
2017
17 2 p. 295-302
artikel
2 A germline missense mutation in exon 3 of the MSH2 gene in a Lynch syndrome family: correlation with phenotype and localization assay Bianchi, Francesca
2017
17 2 p. 215-224
artikel
3 A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families Ghorbanoghli, Zeinab
2017
17 2 p. 209-212
artikel
4 Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing Bijlsma, Rhodé M.
2017
17 2 p. 309-316
artikel
5 Dental anomalies in pediatric patients with familial adenomatous polyposis Septer, Seth
2017
17 2 p. 229-234
artikel
6 Discovery of mutations in homologous recombination genes in African-American women with breast cancer Ding, Yuan Chun
2017
17 2 p. 187-195
artikel
7 Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families Ghorbanoghli, Zeinab
2017
17 2 p. 213
artikel
8 Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations Wang, Tao
2017
17 2 p. 225-228
artikel
9 Issues related to family history of cancer at the end of life: a palliative care providers’ survey Gonthier, Catherine
2017
17 2 p. 303-307
artikel
10 Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan Yousef, Yacoub A.
2017
17 2 p. 261-268
artikel
11 Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin Krivokuca, Ana
2017
17 2 p. 179-185
artikel
12 Pancreatic adenocarcinoma with a germline PTEN p.Arg234Gln mutation Uemura, Sunao
2017
17 2 p. 255-259
artikel
13 Pancreatic neuroendocrine tumor in a patient with a TSC1 variant: case report and review of the literature Mortaji, Parisa
2017
17 2 p. 275-280
artikel
14 p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers Macedo, Gabriel S.
2017
17 2 p. 269-274
artikel
15 Remarkable effects of imatinib in a family with young onset gastrointestinal stromal tumors and cutaneous hyperpigmentation associated with a germline KIT-Trp557Arg mutation: case report and literature overview Farag, S.
2017
17 2 p. 247-253
artikel
16 Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing Alqahtani, Masood
2017
17 2 p. 197-203
artikel
17 Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland Evans, Daniel R.
2017
17 2 p. 205-208
artikel
18 Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations Buecher, Bruno
2017
17 2 p. 281-285
artikel
19 The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes Slavin, Thomas P.
2017
17 2 p. 235-245
artikel
20 Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic Bojadzieva, Jasmina
2017
17 2 p. 287-294
artikel
                             20 gevonden resultaten
 
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