Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
SourceNature Genetics, 17, 3, (1997), pp. 285-291
Article / Letter to editor
Display more detailsDisplay less details
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.