Clinical and molecular genetics of Fraser syndrome
Fraser syndrome (FS MIM 219000) is a rare, heterogeneous congenital malformation disorder characterized by cryptophthalmos, syndactyly and urogenital defects. The entity is named after George Fraser who described two unrelated patients with the same congenital malformation disorder consisting of cry...
| Main Author: | |
|---|---|
| Published: |
University College London (University of London)
2006
|
| Subjects: | |
| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.436374 |