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Does a proactive procedure lead to a higher uptake of predictive testing in families with a pathogenic BRCA1/BRCA2 variant? A family cancer clinic evaluation.
J Genet Couns. 2023 Aug 21. doi: 10.1002/jgc4.1767. Online ahead of print.
J Genet Couns. 2023.
PMID: 37605508
The uptake of predictive DNA testing in 40 families with a pathogenic BRCA1/BRCA2 variant. An evaluation of the proband-mediated procedure.
Menko FH, Jeanson KN, Bleiker EMA, van Tiggelen CWM, Hogervorst FBL, Ter Stege JA, Ait Moha D, van der Kolk LE.
Menko FH, et al. Among authors: jeanson kn.
Eur J Hum Genet. 2020 Aug;28(8):1020-1027. doi: 10.1038/s41431-020-0618-8. Epub 2020 Apr 16.
Eur J Hum Genet. 2020.
PMID: 32300191
Free PMC article.
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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 FH, Ter Stege JA, van der Kolk LE, Jeanson KN, Schats W, Moha DA, Bleiker EMA.
Menko FH, et al. Among authors: jeanson kn.
Fam Cancer. 2019 Jan;18(1):127-135. doi: 10.1007/s10689-018-0089-z.
Fam Cancer. 2019.
PMID: 29846880
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