Mutation in Brief
نویسندگان
چکیده
© 2002 WILEY-LISS, INC. DOI: 10.1002/humu.9036 Received 17 January 2002; revised manuscript accepted 26 February 2002. A HOXA13 Allele With a Missense Mutation in the Homeobox and a Dinucleotide Deletion in the Promoter Underlies Guttmacher Syndrome Jeffrey W. Innis, Frances R. Goodman, Chiara Bacchelli, Thomas M. Williams, Douglas P. Mortlock, Praveen Sateesh, Peter J. Scambler, Wendy McKinnon, and Alan E. Guttmacher
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تاریخ انتشار 2002