Analysis of theFgfr2C342Ymouse model shows condensation defects due to misregulation ofSox9expression in prechondrocytic mesenchyme

Central nervous system and cervical spine abnormalities in Apert syndrome

(2016) Omar Breik et al.   CHILDS NERVOUS SYSTEM

FGFR2c-mediated ERK–MAPK activity regulates coronal suture development

(2016) Miles J. Pfaff et al.   DEVELOPMENTAL BIOLOGY

Tracheal cartilaginous sleeves in children with syndromic craniosynostosis

(2016) Tara L. Wenger et al.   GENETICS IN MEDICINE

Hearing loss in syndromic craniosynostoses: Otologic manifestations and clinical findings

(2014) Nneamaka B. Agochukwu et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

FGF23 Deficiency Leads to Mixed Hearing Loss and Middle Ear Malformation in Mice

(2014) Andrew C. Lysaght et al.   PLoS One

The Fgfr2 W290R mouse model of Crouzon syndrome

(2012) S.-G. Gong   CHILDS NERVOUS SYSTEM

A Sox9/Fgf feed-forward loop maintains pancreatic organ identity

(2012) P. A. Seymour et al.   DEVELOPMENT

Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1

(2012) R. A. Deckelbaum et al.   DEVELOPMENT

Craniosynostosis Associated with Neural Tube Defects: Is There a Causal Association?

(2012) Sachin A. Borkar et al.   PEDIATRIC NEUROSURGERY

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice

(2010) Yingli Wang et al.   BMC DEVELOPMENTAL BIOLOGY

FGF10 controls the patterning of the tracheal cartilage rings via Shh

(2010) F. G. Sala et al.   DEVELOPMENT

Obstructive sleep apnea in children with syndromic craniosynostosis: long-term respiratory outcome of midface advancement

(2010) N. Bannink et al.   INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY

Regulation of Sox9 by Sonic Hedgehog (Shh) is essential for patterning and formation of tracheal cartilage

(2009) Jinhyung Park et al.   DEVELOPMENTAL DYNAMICS

Inner Ear Anomalies and Conductive Hearing Loss in Children With Apert Syndrome

(2009) Guangwei Zhou et al.   OTOLOGY & NEUROTOLOGY

Fibroblast Growth Factor 10 Plays a Causative Role in the Tracheal Cartilage Defects in a Mouse Model of Apert Syndrome

(2009) Caterina Tiozzo et al.   PEDIATRIC RESEARCH

Loss of Fgfr2 leads to partial XY sex reversal

(2007) Stefan Bagheri-Fam et al.   DEVELOPMENTAL BIOLOGY