Apert syndrome: temporal lobe abnormalities on fetal brain imaging

Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia

(2014) D. Pugash et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation

(2013) Cristina M. Philpott et al.   PEDIATRIC RADIOLOGY

Children with Apert Syndrome as Adults

(2013) Robert Tovetjärn et al.   PLASTIC AND RECONSTRUCTIVE SURGERY

The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made

(2013) Nicholas Lench et al.   PRENATAL DIAGNOSIS

Neuroimaging and neurological findings in patients with hypochondroplasia andFGFR3N540K mutation

(2012) Tarja Linnankivi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Central nervous system malformations and deformations inFGFR2-related craniosynostosis

(2012) Roman Hossein Khonsari et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Apert Syndrome in a Newborn Infant Without Craniosynostosis

(2012) Sivaroopi Coomaralingam et al.   JOURNAL OF CRANIOFACIAL SURGERY

FGF Signaling Expands Embryonic Cortical Surface Area by Regulating Notch-Dependent Neurogenesis

(2011) B. G. Rash et al.   JOURNAL OF NEUROSCIENCE

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

(2010) Kristina Aldridge et al.   DEVELOPMENTAL DYNAMICS

Malformation of the fetal brain in thanatophoric dysplasia: US and MRI findings

(2010) A. Michelle Fink et al.   PEDIATRIC RADIOLOGY