Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia
- Resource Type
- Article
- Source
- In
Taiwanese Journal of Obstetrics & Gynecology June 2017 56(3):412-414 - Subject
- Language
- ISSN
- 1028-4559