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A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family.
PMID: 11768390 [PubMed - indexed for MEDLINE]
PMCID: PMC1734788
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Cited by 3 PubMed Central articles
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Genes in glucose metabolism and association with spina bifida.
Davidson CM, Northrup H, King TM, Fletcher JM, Townsend I, Tyerman GH, Au KS.
Reprod Sci. 2008 Jan; 15(1):51-8.
[Reprod Sci. 2008]
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In silico and in vivo splicing analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects.
Lastella P, Surdo NC, Resta N, Guanti G, Stella A.
BMC Genomics. 2006 Sep 22; 7:243. Epub 2006 Sep 22.
[BMC Genomics. 2006]
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PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level.
Conde L, Vaquerizas JM, Santoyo J, Al-Shahrour F, Ruiz-Llorente S, Robledo M, Dopazo J.
Nucleic Acids Res. 2004 Jul 1; 32(Web Server issue):W242-8.
[Nucleic Acids Res. 2004]