Found: 6
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Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.
- Published in:
- Oncogene, 2000, v. 19, n. 13, p. 1719, doi. 10.1038/sj.onc.1203447
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- Article
Three submicroscopic deletions at the APC locus and their rapid detection by quantitative-PCR analysis.
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- European Journal of Human Genetics, 1999, v. 7, n. 6, p. 695, doi. 10.1038/sj.ejhg.5200344
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- Article
Retinoids regulate expression of the retinol-binding protein gene in hepatoma cells in culture.
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- Journal of Cellular Physiology, 1994, v. 160, n. 3, p. 596, doi. 10.1002/jcp.1041600323
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- Article
The mutation spectrum of the APC gene in FAP patients from southern Italy: Detection of known and four novel mutations(Communicated by Mark H. Paalman)Online Citation: Human Mutation, Mutation in Brief #622 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/622.pdf)
- Published in:
- Human Mutation, 2003, v. 21, n. 6, p. 655, doi. 10.1002/humu.9151
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- Article
Familial adenomatous polyposis coli: Five novel mutations in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients.
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- Human Mutation, 1999, v. 13, n. 3, p. 256, doi. 10.1002/(SICI)1098-1004(1999)13:3<256::AID-HUMU13>3.0.CO;2-J
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- Article
A novel Mbo II polymorphism in exon 15 of the human adenomatous polyposis coli gene.
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- Clinical Genetics, 1998, v. 53, n. 4, p. 315, doi. 10.1111/j.1399-0004.1998.tb02704.x
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- Article