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A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
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  1. Dr Foulkes.MDWF{at}musica.mcgill.ca
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YUAN ZQ, WONG N, FOULKES WD, et al
A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening

Publication history

  • First published October 1, 1999.
Online issue publication 
October 01, 1999

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