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Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecularcytogenetic characterization and association with a 1.2-Mb microduplicationat 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with anapparently pure 4p deletion Chen, C.P.;Su, Y.N.;Chen, Y.Y.;Su, J.W.;Chern, S.R.;Chen, Y.T.;Chen, W.L.;Chen, L.F.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2011-12-01 查看
Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecularcytogenetic characterization and association with a 1.2-Mb microduplicationat 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with anapparently pure 4p deletion Chen, C.P.;Su, Y.N.;Chen, Y.Y.;Su, J.W.;Chern, S.R.;Chen, Y.T.;Chen, W.L.;Chen, L.F.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2011-12-01 查看
Detection of recurrent 4p16.3 microdeletion with 2p25.3microduplication by multiplex ligation-dependent probe amplification andarray comparative genomic hybridization in a fetus from a family withWolf-Hirschhorn syndrome Yang, W.X.;Pan, H.;Wang, S.T.;Li, L.;Wu, H.R.;Qi, Y.; Taiwanese Journal of Obstetrics and Gynecology 2016-02-01 查看
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