The AAPC case, with an early onset of colorectal cancer

Author:

Plawski A.,Nowakowska D.,Podralska M.,Lipinski D.,Steffen J.,Slomski R.

Publisher

Springer Science and Business Media LLC

Subject

Gastroenterology

Reference17 articles.

1. Groden J, Thliveris A, Samowitz W et al (1991) Identification and characterization of the familial adenomatous polyposis coli gene. Cell 66:589–600

2. Kinzler KW, Nilbert MC, Su LK et al (1991) Identification of FAP locus genes from chromosome 5q21. Science 253:661–665

3. Nagase H, Miyoshi Y, Horii A et al (1992) Correlation between the location of germ-line mutations in the APC gene and the number of colorectal polyps in familial adenomatous polyposis patients. Cancer Res 52:4055–4057

4. Caspari R, Olschwang S, Friedl W et al (1995) Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444. Hum Mol Genet 4:337–340

5. Caspari R, Friedl W, Boker T et al (1993) Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods. Z Gastroenterol 31:646–652

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