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Page 1
Germline variants and phenotypic spectrum in a Canadian cohort of individuals with diffuse gastric cancer.
Curr Oncol. 2020 Apr;27(2):e182-e190. doi: 10.3747/co.27.5663. Epub 2020 May 1.
Curr Oncol. 2020.
PMID: 32489267
Free PMC article.
Pilot Testing of a Psycho-educational Telephone Intervention for Women Receiving Uninformative BRCA1/2 Genetic Test Results.
Maheu C, Meschino WS, Hu W, Honeyford J, Ambus I, Kidd M, Benea A, Gao X, Azadbakhsh M, Rochefort C, Esplen MJ.
Maheu C, et al. Among authors: ambus i.
Can J Nurs Res. 2015 Mar;47(1):53-71. doi: 10.1177/084456211504700105.
Can J Nurs Res. 2015.
PMID: 29509450
English, French.
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BRCA1/2 predictive testing: a study of uptake in two centres.
Brooks L, Lennard F, Shenton A, Lalloo F, Ambus I, Ardern-Jones A, Belk R, Kerr B, Craufurd D, Eeles R, Gareth Evans D.
Brooks L, et al. Among authors: ambus i.
Eur J Hum Genet. 2004 Aug;12(8):654-62. doi: 10.1038/sj.ejhg.5201206.
Eur J Hum Genet. 2004.
PMID: 15138457
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The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC.
Ollila S, Fitzpatrick R, Sarantaus L, Kariola R, Ambus I, Velsher L, Hsieh E, Andersen MK, Raevaara TE, Gerdes AM, Mangold E, Peltomäki P, Lynch HT, Nyström M.
Ollila S, et al. Among authors: ambus i.
Int J Oncol. 2006 Jan;28(1):149-53.
Int J Oncol. 2006.
PMID: 16327991
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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
Weksberg R, Nishikawa J, Caluseriu O, Fei YL, Shuman C, Wei C, Steele L, Cameron J, Smith A, Ambus I, Li M, Ray PN, Sadowski P, Squire J.
Weksberg R, et al. Among authors: ambus i.
Hum Mol Genet. 2001 Dec 15;10(26):2989-3000. doi: 10.1093/hmg/10.26.2989.
Hum Mol Genet. 2001.
PMID: 11751681
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