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

✍ Scribed by 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

• Book ID: 116920732
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 953 KB
• Volume: 50
• Category: Article
• ISSN: 1028-4559
• DOI: 10.1016/j.tjog.2011.10.019