Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
作者信息
Chadefaux B, Bonnefont J P, Rabier D, Shih V E, Saudubray J M, Kamoun P
出版信息
Am J Med Genet. 1989 Feb;32(2):264. doi: 10.1002/ajmg.1320320228.
PMID:2929667
Abstract
摘要
Zotero 插件