Article
Analysis of intracranial volume in apert syndrome genotypes.
Pediatric neurosurgery - 1 Jan 2000
Anderson Peter J, Netherway David J, Abbott Amanda H, Cox Timothy, Roscioli Tony, David David J
Abstract excerpt
OBJECTIVE: Apert syndrome is caused by a mutation of the fibroblastic growth factor type 2 gene and in nearly all of the cases where the mutation has been identified it occurs in one of two adjacent sites of the gene, either position 252 or position 253. There is currently uncertainty whether a worse neurosurgical outcome occurs in association with a particular genotype. We investigated whether there were...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.