Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes

Beare-Stevenson syndrome: Two new patients, including a novel finding of tracheal cartilaginous sleeve

(2015) Tara L. Wenger et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prenatal diagnosis of Carpenter syndrome: Looking beyond craniosynostosis and polysyndactyly

(2014) Anna S. Victorine et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prenatal findings in carpenter syndrome and a novel mutation inRAB23

(2014) Damien Haye et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Apert syndrome: temporal lobe abnormalities on fetal brain imaging

(2014) Zornitza Stark et al.   PRENATAL DIAGNOSIS

Genotype and clinical care correlations in craniosynostosis: Findings from a cohort of 630 Australian and New Zealand patients

(2013) T. Roscioli et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

A familial case of Muenke syndrome. Diverse expressivity of theFGFR3Pro252Arg mutation – case report and review of the literature

(2013) Christos Aravidis et al.   Journal of Maternal-Fetal & Neonatal Medicine

Prenatal diagnosis of Pfeiffer syndrome prior to 20 weeks’ gestation

(2013) J. L. Gómez-Gómez et al.   JOURNAL OF OBSTETRICS AND GYNAECOLOGY

Central nervous system malformations and deformations inFGFR2-related craniosynostosis

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

Parameters of care for craniosynostosis: Dental and orthodontic perspectives

(2012) Karin Vargervik et al.   AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS

Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre–Chotzen syndrome

(2012) Emmanuel Spaggiari et al.   European Journal of Medical Genetics

Apert Syndrome with Fused Thalami

(2012) Kathrin Ludwig et al.   Fetal and Pediatric Pathology

Craniosynostosis

(2011) David Johnson et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Tracheobronchial Anomalies in Syndromic Craniosynostosis With 3-Dimensional CT Image and Bronchoscopy

(2011) Takuya Fujimoto et al.   JOURNAL OF CRANIOFACIAL SURGERY

Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature

(2010) Gabriele Tonni et al.   ARCHIVES OF GYNECOLOGY AND OBSTETRICS

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

Spectrum of Antley-Bixler Syndrome

(2010) Karen L. McGlaughlin et al.   JOURNAL OF CRANIOFACIAL SURGERY

Tracheal cartilaginous sleeve in patients with craniosynostosis syndromes: a meta-analysis

(2010) Keith Lertsburapa et al.   JOURNAL OF PEDIATRIC SURGERY

Second-trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18

(2010) Chih-Ping Chen et al.   Taiwanese Journal of Obstetrics & Gynecology

Prenatal MRI Findings of Fetuses with Congenital High Airway Obstruction Sequence

(2009) Carolina V. A. Guimaraes et al.   KOREAN JOURNAL OF RADIOLOGY

A population-based study of craniosynostosis in metropolitan Atlanta, 1989–2003

(2008) Sheree L. Boulet et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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