A HOXA13 allele with a missense mutation in the homeobox...

Human Mutation 2002 Vol. 19; Iss. 5

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, Alan E. Guttmacher
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Volume:
19
Year:
2002
Language:
english
Pages:
2
DOI:
10.1002/humu.9036
File:
PDF, 166 KB
english, 2002
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