A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening

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Bibliographic Details
Published in:Journal of medical genetics 1999-10, Vol.36 (10), p.792-793
Main Authors: YUAN, Z. Q., WONG, N., FOULKES, W., ALPERT, L., MANGANARO, F., ANDREUTTI-ZAUGG, C., IGGO, R., ANTHONY, K., HSIEH, E., REDSTON, M., PINSKY, L., TRIFIRO, M., GORDON, P., LASKO, D.
Format: Article
Language:English
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ISSN:0022-2593
1468-6244