Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case

Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome

(2011) Patrick K. C. Au et al.   PRENATAL DIAGNOSIS

Fetal magnetic resonance imaging: indications, study protocols and safety

(2011) F. Triulzi et al.   Radiologia Medica

Germinal mosaicism in Apert syndrome

(2010) Judith E. Allanson   CLINICAL GENETICS

Prenatal Diagnosis of Apert Syndrome with Cloverleaf Skull Deformity Using Ultrasound, Fetal Magnetic Resonance Imaging and Genetic Analysis

(2010) Benedikt Weber et al.   FETAL DIAGNOSIS AND THERAPY

Role of fetal MRI in the diagnosis of cerebral ventriculomegaly assessed by ultrasonography

(2009) L. Manganaro et al.   Radiologia Medica

Monozygotic Twins with Apert Syndrome

(2008) Corstiaan C. Breugem et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

Apert Syndrome: The Current Role of Prenatal Ultrasound and Genetic Analysis in Diagnosis and Counselling

(2008) A.P. Athanasiadis et al.   FETAL DIAGNOSIS AND THERAPY