Pfeiffer syndrome: literature review of prenatal sonographic findings and genetic diagnosis

Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes

(2016) Eva I. Rubio et al.   PEDIATRIC RADIOLOGY

Pfeiffer syndrome: the importance of prenatal diagnosis

(2014) Gatske M. Nieuwenhuyzen-De Boer et al.   European Journal of Obstetrics & Gynecology and Reproductive Biology

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

Three-dimensional features of Pfeiffer syndrome

(2009) Margarita Medina et al.   INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS

A c.1019A > G mutation inFGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygia

(2008) Gareth Baynam et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A rare case of Pfeiffer's syndrome

(2008) P. Pallagatti et al.   JOURNAL OF OBSTETRICS AND GYNAECOLOGY