Detalhe da pesquisa
1.
High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.
Hum Mutat
; 30(8): E797-812, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19459153
2.
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.
Fam Cancer
; 5(1): 21-8, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16528605