Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: Prenatal diagnosis and aCGH characterization using uncultured amniocytes

✍ Scribed by Chen, Chih-Ping; Huang, Jian-Pei; Chen, Yi-Yung; Chern, Schu-Rern; Wu, Peih-Shan; Su, Jun-Wei; Pan, Chen-Wen; Wang, Wayseen

• Book ID: 125454715
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 586 KB
• Volume: 527
• Category: Article
• ISSN: 0378-1119
• DOI: 10.1016/j.gene.2013.06.081