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A missense mutation in both Msh2 and Apc in an Ashkenazi Jewish Hnpcc kindred: Implication for clinical screening
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Yuan, A., Wong, N., Foulkes, W.D., Albert, L., Manganaro F., Andreutti-Zaugg, C., Iggo, R., Anthony, K., Hsieh, E., Redston, M., Pinsky, L., Trifiro, M., Gordon, P.H., and Lasko, D. (1999). A missense mutation in both Msh2 and Apc in an Ashkenazi Jewish Hnpcc kindred: Implication for clinical screening. J. Med. Genet. 36, 790-793.
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Yuan, A.1
Wong, N.2
Foulkes, W.D.3
Albert, L.4
Manganaro, F.5
Andreutti-Zaugg, C.6
Iggo, R.7
Anthony, K.8
Hsieh, E.9
Redston, M.10
Pinsky, L.11
Trifiro, M.12
Gordon, P.H.13
Lasko, D.14
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