A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening.
作者信息
Yuan Z Q, Wong N, Foulkes W D, Alpert L, Manganaro F, Andreutti-Zaugg C, Iggo R, Anthony K, Hsieh E, Redston M, Pinsky L, Trifiro M, Gordon P H, Lasko D
出版信息
J Med Genet. 1999 Oct;36(10):790-3. doi: 10.1136/jmg.36.10.792.
Abstract
摘要
Zotero 插件