Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold

✍ Scribed by Chen, Chih-Ping; Chen, Yi-Yung; Chern, Schu-Rern; Wu, Peih-Shan; Su, Jun-Wei; Chen, Yu-Ting; Chen, Li-Feng; Wang, Wayseen

• Book ID: 123457744
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 864 KB
• Volume: 516
• Category: Article
• ISSN: 0378-1119
• DOI: 10.1016/j.gene.2012.12.051