A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX
- Resource Type
- Article
- Authors
- Ansari, Morad; Rainger, Jacqueline K.; Murray, Jennie E.; Hanson, Isabel; Firth, Helen V.; Mehendale, Felicity; Amiel, Jeanne; Gordon, Christopher T.; Percesepe, Antonio; Mazzanti, Laura; Fryer, Alan; Ferrari, Paola; Devriendt, Koenraad; Temple, I. Karen; FitzPatrick, David R.
- Source
- In European Journal of Medical Genetics October 2014 57(10):587-595
- Subject
- Language
- ISSN
- 1769-7212