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                             20 results found
no title author magazine year volume issue page(s) type
1 Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma Donner, Iikki
2018
18 1 p. 113-119
article
2 Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variant Bonis, Maria De
2018
18 1 p. 29-35
article
3 Cholesterol profile in women with premature menopause after risk reducing salpingo-oophorectomy Teixeira, Natalia
2018
18 1 p. 19-27
article
4 Clinical and pathologic characteristics of breast cancer patients carrying the c.3481_3491del11 mutation El Tannouri, R.
2018
18 1 p. 1-8
article
5 Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer Bush, Lisa
2018
18 1 p. 105-108
article
6 Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori Hakkaart, Christopher
2018
18 1 p. 83-90
article
7 Hemangioblastoma in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome: a phenotypic overlap between VHL and HLRCC Syndromes Dow, Eryn
2018
18 1 p. 91-95
article
8 Identification of a novel GREM1 duplication in a patient with multiple colon polyps McKenna, Danielle B.
2018
18 1 p. 63-66
article
9 Low-level parental mosaicism in an apparent de novo case of Peutz–Jeghers syndrome Butel-Simoes, G. I.
2018
18 1 p. 109-112
article
10 Modified capture–recapture estimates of the number of families with Lynch syndrome in Central Ohio Ranola, John Michael O.
2018
18 1 p. 67-73
article
11 Outcome of thyroid ultrasound screening in FAP patients with a normal baseline exam Monachese, Marc
2018
18 1 p. 75-82
article
12 Physician interpretation of variants of uncertain significance Macklin, Sarah K.
2018
18 1 p. 121-126
article
13 Prevalence of thyroid diseases in familial adenomatous polyposis: a systematic review and meta-analysis Chenbhanich, Jirat
2018
18 1 p. 53-62
article
14 Reminders of cancer risk and pain catastrophizing: relationships with cancer worry and perceived risk in women with a first-degree relative with breast cancer Whitney, Colette A.
2018
18 1 p. 9-18
article
15 Report of a bi-allelic truncating germline mutation in TP53 Brown, Natasha J.
2018
18 1 p. 101-104
article
16 Sarcoma in neurofibromatosis 2: case report and review of the literature Linder, C.
2018
18 1 p. 97-100
article
17 The BRCA1 exon 13 duplication: clinical characteristics of 22 families in Northern Sweden Edwinsdotter Ardnor, Christina
2018
18 1 p. 37-42
article
18 The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study Reumkens, Kelly
2018
18 1 p. 137-146
article
19 The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice Menko, Fred H
2018
18 1 p. 127-135
article
20 Unsolicited information letters to increase awareness of Lynch syndrome and familial colorectal cancer: reactions and attitudes Petersen, Helle Vendel
2018
18 1 p. 43-51
article
                             20 results found
 
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