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Page 1
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: kasprzak l. Hum Mutat. 2009 Aug;30(8):E797-812. doi: 10.1002/humu.21056. Hum Mutat. 2009. PMID: 19459153
Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.
Castellsagué E, Liu J, Volenik A, Giroux S, Gagné R, Maranda B, Roussel-Jobin A, Latreille J, Laframboise R, Palma L, Kasprzak L, Marcus VA, Breguet M, Nolet S, El-Haffaf Z, Australie K, Gologan A, Aleynikova O, Oros-Klein K, Greenwood C, Mes-Masson AM, Provencher D, Tischkowitz M, Chong G, Rousseau F, Foulkes WD. Castellsagué E, et al. Among authors: kasprzak l. Clin Genet. 2015 Jun;87(6):536-42. doi: 10.1111/cge.12526. Epub 2014 Nov 22. Clin Genet. 2015. PMID: 25318681
A survey of APC mutations in Quebec.
Jarry J, Brunet JS, Laframboise R, Drouin R, Latreille J, Richard C, Gekas J, Maranda B, Monczak Y, Wong N, Pouchet C, Zaor S, Kasprzak L, Palma L, Wu MK, Tischkowitz M, Foulkes WD, Chong G. Jarry J, et al. Among authors: kasprzak l. Fam Cancer. 2011 Dec;10(4):659-65. doi: 10.1007/s10689-011-9468-4. Fam Cancer. 2011. PMID: 21779980
Forth nightly review: hereditary ovarian carcinoma.
Kasprzak L, Foulkes WD, Shelling AN. Kasprzak L, et al. BMJ. 1999 Mar 20;318(7186):786-9. doi: 10.1136/bmj.318.7186.786. BMJ. 1999. PMID: 10082707 Free PMC article. Review. No abstract available.
Multiple primary malignancies in a patient with situs ambiguus.
Galiatsatos P, Kasprzak L, Chong G, Jass JR, Foulkes WD. Galiatsatos P, et al. Among authors: kasprzak l. Clin Genet. 2006 Jun;69(6):528-31. doi: 10.1111/j.1399-0004.2006.00622.x. Clin Genet. 2006. PMID: 16712706 Review. No abstract available.
22 results