Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12-Related Craniosynostosis.
- Resource Type
- Article
- Source
- Human Mutation; Aug2016, Vol. 37 Issue 8, p732-736, 5p
- Subject
- Language
- ISSN
- 10597794