A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening.
Yuan ZQ, Wong N, Foulkes WD, Alpert L, Manganaro F, Andreutti-Zaugg C, Iggo R, Anthony K, Hsieh E, Redston M, Pinsky L, Trifiro M, Gordon PH, Lasko D.
Yuan ZQ, et al. Among authors: foulkes wd.
J Med Genet. 1999 Oct;36(10):790-3. doi: 10.1136/jmg.36.10.792.
J Med Genet. 1999.
PMID: 10528862
Free PMC article.
No abstract available.