FGFR-associated craniosynostosis syndromes and gastrointestinal defects

Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction

(2015) Edward P. Carter et al.   TRENDS IN CELL BIOLOGY

Malrotation and intestinal atresias

(2014) Stephen D. Adams et al.   EARLY HUMAN DEVELOPMENT

Clinical expression in Pfeiffer syndrome type 2 and 3: Surveillance in Japan

(2012) Hiroshi Koga et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

FGF/FGFR signaling in bone formation: Progress and perspectives

(2012) Pierre J. Marie et al.   GROWTH FACTORS

A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome

(2011) Aimee L Fenwick et al.   BMC Medical Genetics

Craniosynostosis

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

Intestinal Mai rotation in a Patient with Pfeiffer Syndrome Type 2

(2010) Yuri A. Zarate et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling

(2010) S. Mai et al.   DEVELOPMENTAL DYNAMICS

Chiari Type 1 Malformation in an Infant With Type 2 Pfeiffer Syndrome

(2010) Adrianna Ranger et al.   JOURNAL OF CRANIOFACIAL SURGERY

Review of genetic factors in intestinal malrotation

(2010) Vicki Martin et al.   PEDIATRIC SURGERY INTERNATIONAL

Intestinal malrotation: Varied clinical presentation from infancy through adulthood

(2010) Deepika Nehra et al.   SURGERY