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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of contralateral breast cancer and skin cancer associated with NBN heterozygous pathogenic variant c.698_701delAACA Gass, Jennifer
2017
16 4 p. 551-553
artikel
2 All in the family? Communication of cancer survivors with their families Bowen, Deborah J.
2017
16 4 p. 597-603
artikel
3 A new POT1 germline mutation—expanding the spectrum of POT1-associated cancers Wilson, Tremika Le-Shan
2017
16 4 p. 561-566
artikel
4 A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families Llovet, Patricia
2017
16 4 p. 567-575
artikel
5 A Peutz–Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report Chiang, Jy-Ming
2017
16 4 p. 555-560
artikel
6 Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria González-Acosta, Maribel
2017
16 4 p. 501-507
artikel
7 General practitioner attitudes towards prescribing aspirin to carriers of Lynch Syndrome: findings from a national survey Smith, Samuel G.
2017
16 4 p. 509-516
artikel
8 Genetic polymorphisms of NFκB1-94ins/delATTG and NFκBIA-881A/G genes in Egyptian patients with colorectal cancer Youssef, Mohamed Ragab
2017
16 4 p. 517-524
artikel
9 High-risk individuals’ perceptions of reproductive genetic testing for CDH1 mutations Hallowell, Nina
2017
16 4 p. 531-535
artikel
10 Identification of novel potential genetic predictors of urothelial bladder carcinoma susceptibility in Pakistani population Ali, Syeda Hafiza Benish
2017
16 4 p. 577-594
artikel
11 Importance of updating family cancer history in childhood cancer survivors Russo, Selena
2017
16 4 p. 605-610
artikel
12 Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancer Lee, Y. C.
2017
16 4 p. 461-469
artikel
13 Inherited DNA repair gene mutations detected by tumor next generation sequencing in urinary tract cancers Gupta, Sumati
2017
16 4 p. 545-550
artikel
14 Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6 Morak, Monika
2017
16 4 p. 491-500
artikel
15 Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series Kidambi, Trilokesh D.
2017
16 4 p. 537-543
artikel
16 Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical–pathological features in BRCA carriers and non-carriers Gabaldó Barrios, Xavier
2017
16 4 p. 477-489
artikel
17 Placing negative multi-gene panel results into clinical context Hermel, David J.
2017
16 4 p. 595
artikel
18 Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes Rosenthal, Elisabeth A.
2017
16 4 p. 611-620
artikel
19 Prevalence of two BRCA1 mutations, 5382insC and 300T > G, in ovarian cancer patients from Ukraine Gorodetska, I.
2017
16 4 p. 471-476
artikel
20 Universal screening for microsatellite instability in colorectal cancer in the clinical genomics era: new recommendations, methods, and considerations Hechtman, Jaclyn F.
2017
16 4 p. 525-529
artikel
                             20 gevonden resultaten
 
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