A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00390.x/fullpdf
Reference14 articles.
1. Sporadic bilateral retinoblastoma and 13q-chromosomal deletion;Francke;Med Pediatr Oncol,1976
2. Gardner syndrome in a man with an interstitial deletion of 5q;Herrera;Am J Med Genet,1986
3. The tumour spectrum in hereditary non-polyposis colorectal cancer: a study of 24 kindreds in the Netherlands;Vasen;Int J Cancer,1990
4. Colorectal carcinoma in different age groups: a population-based investigation;Fante;Am J Gastroenterol,1997
5. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification;Schouten;Nucleic Acids Res,2002
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