Prenatal diagnosis and identification of heterozygous frameshift mutation in PRRX1 in an infant with agnathia-otocephaly.
作者信息
Donnelly Meghan, Todd Emily, Wheeler Marsha, Winn Virginia D, Kamnasaran Deepak
出版信息
Prenat Diagn. 2012 Sep;32(9):903-5. doi: 10.1002/pd.3910. Epub 2012 Jun 5.
DOI:10.1002/pd.3910
PMID:22674740
Abstract
摘要
Zotero 插件