A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies
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E.M.J. has nothing to disclose. J.I.R. has nothing to disclose. L.D. has nothing to disclose. H.S.T. has nothing to disclose.
Supported by National Institute of Environmental Health Sciences grants ES010610 and U54 HD052668.
PII: S0015-0282(09)01205-9
doi:10.1016/j.fertnstert.2009.05.057
© 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

