About this Medicine article
Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies by Ma, Lijiang; Selamet Tierney, Elif Seda; Lee, Teresa; Lanzano, Patricia; Chung, Wendy K. is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Ma, Lijiang; Selamet Tierney, Elif Seda; Lee, Teresa; Lanzano, Patricia; Chung, Wendy K.
- Publisher
- Cambridge University Press; Cambridge University Press (CUP) (ISSN 1047-9511)
- Published
- 2011
- Field
- Medicine (Health Sciences)