Search
Now showing items 1-2 of 2
Patterns of brain growth in one FGFR2 mouse model for Apert Syndrome
(2010)
Apert syndrome is a disorder associated with craniosynostosis resulting from one of two mutations in Fibroblast Growth Factor Receptor 2 (FGFR2). Individuals with Apert syndrome demonstrate brain dysmorphology, often ...
Intracranial and whole brain volumes in infants with sagittal craniosynostosis
(2010)
Single-suture craniosynostosis occurs in approximately1 in 2000 live births and has been associated with brain dysmorphology. It has been suggested that premature fusion of cranial sutures restricts and alters brain growth ...