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

• Main Authors: Chih-Ping Chen (Author), Yi-Ning Su (Author), Yi-Yung Chen (Author), Jun-Wei Su (Author), Schu-Rern Chern (Author), Yu-Ting Chen (Author), Wen-Lin Chen (Author), Li-Feng Chen (Author), Wayseen Wang (Author)
• Format: Book
• Published: Elsevier, 2011-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Objective: To present prenatal diagnosis and molecular cytogenetic characterization of Wolf-Hirschhorn syndrome (WHS) associated with microduplications at 8p and 10p in a fetus with an apparently pure 4p deletion. Case Report: A 35-year-old gravida 2, para 1 woman underwent amniocentesis at 18 weeks...