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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.
Wagner A, Barrows A, Wijnen JT, van der Klift H, Franken PF, Verkuijlen P, Nakagawa H, Geugien M, Jaghmohan-Changur S, Breukel C, Meijers-Heijboer H, Morreau H, van Puijenbroek M, Burn J, Coronel S, Kinarski Y, Okimoto R, Watson P, Lynch JF, de la Chapelle A, Lynch HT, Fodde R. Wagner A, et al. Among authors: watson p. Am J Hum Genet. 2003 May;72(5):1088-100. doi: 10.1086/373963. Epub 2003 Mar 25. Am J Hum Genet. 2003. PMID: 12658575 Free PMC article.
Hereditary nonpolyposis colorectal cancer--Lynch syndromes I and II.
Lynch HT, Lanspa SJ, Boman BM, Smyrk T, Watson P, Lynch JF, Lynch PM, Cristofaro G, Bufo P, Tauro AV, et al. Lynch HT, et al. Among authors: watson p. Gastroenterol Clin North Am. 1988 Dec;17(4):679-712. Gastroenterol Clin North Am. 1988. PMID: 3068137 Review.
Surveillance in Lynch syndrome: how aggressive?
Lanspa SJ, Jenkins JX, Cavalieri RJ, Smyrk TC, Watson P, Lynch J, Lynch HT. Lanspa SJ, et al. Among authors: watson p. Am J Gastroenterol. 1994 Nov;89(11):1978-80. Am J Gastroenterol. 1994. PMID: 7942721
2,434 results