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                             14 results found
no title author magazine year volume issue page(s) type
1 A comprehensive reference for BRCA1/2 genes pathogenic variants in Iran: published, unpublished and novel Majidzadeh-A, Keivan

21 2 p. 137-142
article
2 Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population Mittendorf, Kathleen F.

21 2 p. 167-180
article
3 A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancer Kedar, I.

21 2 p. 181-188
article
4 CDH1 pathogenic variants and cancer risk in an unselected patient population Bar-Mashiah, Ariel

21 2 p. 235-239
article
5 Extended gene panel testing in lobular breast cancer van Veen, Elke M.

21 2 p. 129-136
article
6 First international workshop of the ATM and cancer risk group (4-5 December 2019) Lesueur, Fabienne

21 2 p. 211-227
article
7 “I wish that there was more info”: characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variants Reyes, Kathryn G.

21 2 p. 143-155
article
8 Malignancy risk in individuals with familial adenomatous polyposis receiving biologics and immunomodulators Faisal, Muhammad Salman

21 2 p. 189-195
article
9 Pilot study of an online training program to increase genetic literacy and communication skills in oncology healthcare professionals discussing BRCA1/2 genetic testing with breast and ovarian cancer patients Meiser, Bettina

21 2 p. 157-166
article
10 Questioning the validity of clinically available breast cancer polygenic risk scores: comparison of two labs reveals discrepancies Wynn, Julia

21 2 p. 125-127
article
11 Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations? Ludman, Mark D.

21 2 p. 121-123
article
12 The clinical features of polymerase proof-reading associated polyposis (PPAP) and recommendations for patient management Palles, Claire

21 2 p. 197-209
article
13 The psychological impact and experience of breast cancer screening in young women with an increased risk of breast cancer due to neurofibromatosis type 1 Crook, Ashley

21 2 p. 241-253
article
14 Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblings Fugaru, Ioana

21 2 p. 229-233
article
                             14 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands