A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome
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F.J.S.C. has nothing to disclose. A.B.T. has nothing to disclose. R.W.P. has nothing to disclose. M.S.A. has nothing to disclose.
PII: S0015-0282(09)03509-2
doi:10.1016/j.fertnstert.2009.08.034
© 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

