Related references
Note: Only part of the references are listed.Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction
Edward P. Carter et al.
TRENDS IN CELL BIOLOGY (2015)
Malrotation and intestinal atresias
Stephen D. Adams et al.
EARLY HUMAN DEVELOPMENT (2014)
Clinical Expression in Pfeiffer Syndrome Type 2 and 3: Surveillance in Japan
Hiroshi Koga et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
FGF/FGFR signaling in bone formation: Progress and perspectives
Pierre J. Marie et al.
GROWTH FACTORS (2012)
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
Aimee L. Fenwick et al.
BMC MEDICAL GENETICS (2011)
Craniosynostosis
David Johnson et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Intestinal malrotation: Varied clinical presentation from infancy through adulthood
Deepika Nehra et al.
SURGERY (2011)
Intestinal Malrotation in a Patient With Pfeiffer Syndrome Type 2
Yuri A. Zarate et al.
CLEFT PALATE-CRANIOFACIAL JOURNAL (2010)
The Missense Mutation W290R in Fgfr2 Causes Developmental Defects From Aberrant IIIb and IIIc Signaling
S. Mai et al.
DEVELOPMENTAL DYNAMICS (2010)
Chiari Type 1 Malformation in an Infant With Type 2 Pfeiffer Syndrome: Further Evidence of Acquired Pathogenesis
Adrianna Ranger et al.
JOURNAL OF CRANIOFACIAL SURGERY (2010)
Review of genetic factors in intestinal malrotation
Vicki Martin et al.
PEDIATRIC SURGERY INTERNATIONAL (2010)
Ocular abnormalities in Apert syndrome: Genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations
Suzanne K. Jadico et al.
JOURNAL OF AAPOS (2006)
Sonographic prenatal diagnosis of malpositioned stomach as a feature of uncomplicated intestinal malrotation
M Cassart et al.
PEDIATRIC RADIOLOGY (2006)
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome
E Lajeunie et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Cellular signaling by fibroblast growth factor receptors
VP Eswarakumar et al.
CYTOKINE & GROWTH FACTOR REVIEWS (2005)
Disorders of intestinal rotation and fixation (malrotation)
PJ Strouse
PEDIATRIC RADIOLOGY (2004)
Fibroblast growth factor receptor 2 IIIb invalidation - A potential cause of familial duodenal atresia
TJ Fairbanks et al.
JOURNAL OF PEDIATRIC SURGERY (2004)
Malformations of the craniofacial region: Evolutionary, embryonic, genetic, and clinical perspectives
MM Cohen
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Intestinal malrotation in adolescents and adults: Spectrum of clinical and imaging features
PJ Pickhardt et al.
AMERICAN JOURNAL OF ROENTGENOLOGY (2002)
Severe and mild phenotypes in Pfeiffer syndrome with splice acceptor mutations in exon IIIc of FGFR2
AS Teebi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome
OA Ibrahimi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Crystal structures of two FGF-FGFR complexes reveal the determinants of ligand-receptor specificity
AN Plotnikov et al.
CELL (2000)
Clustering of FGFR2 gene mutations in patients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses)
W Kress et al.
CYTOGENETICS AND CELL GENETICS (2000)
Share Paper
