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1996 | 1 |
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Page 1
Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.
Clin Genet. 2015 Jun;87(6):536-42. doi: 10.1111/cge.12526. Epub 2014 Nov 22.
Clin Genet. 2015.
PMID: 25318681
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.
Chong G, Jarry J, Marcus V, Thiffault I, Winocour S, Monczak Y, Drouin R, Latreille J, Australie K, Bapat B, Gordon PH, Giguère Y, Gologan A, Galiatsatos P, Jass JR, Wong N, Zaor S, Palma L, Kasprzak L, Tischkowitz M, Foulkes WD.
Chong G, et al. Among authors: australie k.
Hum Mutat. 2009 Aug;30(8):E797-812. doi: 10.1002/humu.21056.
Hum Mutat. 2009.
PMID: 19459153
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Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria.
Brooks-Wilson AR, Kaurah P, Suriano G, Leach S, Senz J, Grehan N, Butterfield YS, Jeyes J, Schinas J, Bacani J, Kelsey M, Ferreira P, MacGillivray B, MacLeod P, Micek M, Ford J, Foulkes W, Australie K, Greenberg C, LaPointe M, Gilpin C, Nikkel S, Gilchrist D, Hughes R, Jackson CE, Monaghan KG, Oliveira MJ, Seruca R, Gallinger S, Caldas C, Huntsman D.
Brooks-Wilson AR, et al. Among authors: australie k.
J Med Genet. 2004 Jul;41(7):508-17. doi: 10.1136/jmg.2004.018275.
J Med Genet. 2004.
PMID: 15235021
Free PMC article.
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The value of multi-modal gene screening in HNPCC in Quebec: three mutations in mismatch repair genes that would have not been correctly identified by genomic DNA sequencing alone.
McVety S, Li L, Thiffault I, Gordon PH, Macnamara E, Wong N, Australie K, Kasprzak L, Chong G, Foulkes WD.
McVety S, et al. Among authors: australie k.
Fam Cancer. 2006;5(1):21-8. doi: 10.1007/s10689-005-2572-6.
Fam Cancer. 2006.
PMID: 16528605
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Parental attitudes to genetic counseling and predictive testing for childhood cancer.
Malkin D, Australie K, Shuman C, Barrera M, Weksberg R.
Malkin D, et al. Among authors: australie k.
Am J Hum Genet. 1996 Oct;59(4):A7.
Am J Hum Genet. 1996.
PMID: 11644836
No abstract available.
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