Author/Creator: Hamel, N - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Hamel, N

1. An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1. Issue 5 (1st May 2002)

Authors:: Hutter, P; Wijnen, J; Rey-Berthod, C; Thiffault, I; Verkuijlen, P; Farber, D; Hamel, N; Bapat, B; Thibodeau, S N; Burn, J; Wu, J; MacNamara, E; Heinimann, K; Chong, G; Foulkes, W D
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 5(2002)
Page Start:: 323
Record Type:: Journal Article
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2. BRCA1:185delAG found in the San Luis Valley probably originated in a Jewish founder. Issue 5 (29th April 2005)

Authors:: Makriyianni, I; Hamel, N; Ward, S; Foulkes, W D; Graw, S
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 5(2005)
Page Start:: e27
Record Type:: Journal Article
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3. The HNPCC associated MSH2*1906G→C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population. Issue 10 (30th September 2005)

Authors:: Sun, S; Greenwood, C M T; Thiffault, I; Hamel, N; Chong, G; Foulkes, W D
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 10(2005)
Page Start:: 766
Record Type:: Journal Article
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4. The RNASEL 471delAAAG allele and prostate cancer in Ashkenazi Jewish men. Issue 3 (1st March 2003)

Authors:: Kotar, K; Hamel, N; Thiffault, I; Foulkes, W D
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 3(2003)
Page Start:: e22
Record Type:: Journal Article
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