Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/1554

Title:	Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion
Authors:	Chih-Ping Chen;Yi-Ning Su;Yi-Yung Chen;Jun-Wei Su;Schu-Rern Chern;Yu-Ting Chen;Wen-Lin Chen;Li-Feng Chen;Wayseen Wang.
Contributors:	生醫所
Date:	2011-12-01
Issue Date:	2015-03-16 15:48:53 (UTC+8)
Relation:	Taiwanese Journal of Obstetrics and Gynecology 50，506-511
Appears in Collections:	[Institute of Biomedical Sciences] Journal papers

Files in This Item:

There are no files associated with this item.