A survey of APC mutations in Quebec
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W. Foulkes | J. Brunet | R. Drouin | B. Maranda | M. Tischkowitz | R. Laframboise | J. Latreille | J. Jarry | C. Richard | J. Gekas | Y. Monczak | N. Wong | C. Pouchet | Sonya Zaor | L. Kasprzak | L. Palma | M. Wu | G. Chong | Mona K. Wu | Laura Palma
[1] C. Lázaro,et al. Detection of genetic alterations in hereditary colorectal cancer screening. , 2010, Mutation research.
[2] Matthew Mort,et al. The Human Gene Mutation Database: providing a comprehensive central mutation database for molecular diagnostics and personalised genomics , 2009, Human Genomics.
[3] W. Foulkes,et al. High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families , 2009, Human mutation.
[4] Á. Carracedo,et al. Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations? , 2009, BMC Medical Genetics.
[5] K. Heimdal,et al. APC mutation spectrum of Norwegian familial adenomatous polyposis families: high ratio of novel mutations , 2009, Journal of Cancer Research and Clinical Oncology.
[6] H. Grönberg,et al. Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families , 2008, BMC medicine.
[7] M. Nieuwenhuis,et al. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature. , 2007, Critical reviews in oncology/hematology.
[8] P. Propping,et al. A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification. , 2007, The Journal of molecular diagnostics : JMD.
[9] B. Yoo,et al. Mutation spectrum of the APC gene in 83 Korean FAP families , 2005, Human mutation.
[10] Thierry Soussi,et al. UMD (Universal Mutation Database): 2005 update , 2005, Human mutation.
[11] J. Vermeesch,et al. Large deletions of the APC gene in 15% of mutation‐negative patients with classical polyposis (FAP): A Belgian study , 2005, Human mutation.
[12] P. Propping,et al. Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis , 2005, Journal of Medical Genetics.
[13] D. Eccles,et al. Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification , 2004, British Journal of Cancer.
[14] K. Halling,et al. First genotype characterization of Argentinean FAP patients: Identification of 14 novel APCmutations , 2004, Human mutation.
[15] G. Riegler,et al. The mutation spectrum of the APC gene in FAP patients from southern Italy: Detection of known and four novel mutations , 2003, Human mutation.
[16] P. Radice,et al. Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] D. Zwijnenburg,et al. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. , 2002, Nucleic acids research.
[18] J. Gebert,et al. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families , 2001, Gut.
[19] I Tomlinson,et al. Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q. , 2000, Human molecular genetics.
[20] S. Powell,et al. Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene , 1998, Gut.
[21] Z. Cohen,et al. Genotype-phenotype correlations in attenuated adenomatous polyposis coli. , 1998, American journal of human genetics.
[22] Rodney J. Scott,et al. Germline mutations in the 3′ part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli , 1996, Human Genetics.
[23] P. Propping,et al. Attenuated familial adenomatous polyposis due to a mutation in the 3′ part of the APC gene. A clue for understanding the function of the APC protein , 1996, Human Genetics.
[24] W. Bodmer,et al. Phenotypic expression in familial adenomatous polyposis: partial prediction by mutation analysis. , 1994, Gut.
[25] G. Thomas,et al. Alleles of the APC gene: An attenuated form of familial polyposis , 1993, Cell.
[26] L. Lipton,et al. The genetics of FAP and FAP-like syndromes , 2005, Familial Cancer.
[27] S Rozen,et al. Primer3 on the WWW for general users and for biologist programmers. , 2000, Methods in molecular biology.
[28] Thierry Soussi,et al. APC gene: database of germline and somatic mutations in human tumors and cell lines , 1996, Nucleic Acids Res..