Add to ORKGApert Syndrome (AS) is one of several fibroblast growth factor receptor (FGFR) related craniosynostosis syndromes. Individuals with AS display craniofacial dysmorphology and a constellation of central nervous system anomalies. In this study we present quantitative comparisons of brain phenotypes in a mouse model for Apert syndrome, the Fgfr2+/S252W mouse
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities,...
WOS: 000425647900009PubMed ID: 29483804Apert syndrome is an autosomal dominant craniosynostosis synd...
Apert syndrome is an autosomal dominantly inherited disorder caused by missense mutations in fibrobl...
Apert syndrome (AS) is one of at least nine disorders considered members of the FGFR-1, -2, and -3-r...
Apert syndrome (AS) is one of at least nine disorders considered members of the fibroblast growth fa...
Apert syndrome is a disorder associated with craniosynostosis resulting from one of two mutations in...
Apert syndrome (AS), the most severe form craniosynostosis, is characterized by premature fusion of ...
<div><p>Apert syndrome (AS), the most severe form craniosynostosis, is characterized by premature fu...
The fibroblast growth factor and receptor system (FGF/FGFR) mediates cell communication and pattern ...
The form and function of the craniofacial structure critically depend on genetic information. With r...
SUMMARY Apert syndrome is a congenital disorder characterized by severe skull malformations and caus...
Apert syndrome (AS), the most severe form of craniosynostosis, is caused by missense mutations inclu...
Objective: Activating mutations in the fibroblast growth factor receptor-2 (FGFR2) have been shown t...
Apert syndrome is a rare genetic disorder characterized by craniosynostosis, midface retrusion, and ...
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities,...
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities,...
WOS: 000425647900009PubMed ID: 29483804Apert syndrome is an autosomal dominant craniosynostosis synd...
Apert syndrome is an autosomal dominantly inherited disorder caused by missense mutations in fibrobl...
Apert syndrome (AS) is one of at least nine disorders considered members of the FGFR-1, -2, and -3-r...
Apert syndrome (AS) is one of at least nine disorders considered members of the fibroblast growth fa...
Apert syndrome is a disorder associated with craniosynostosis resulting from one of two mutations in...
Apert syndrome (AS), the most severe form craniosynostosis, is characterized by premature fusion of ...
<div><p>Apert syndrome (AS), the most severe form craniosynostosis, is characterized by premature fu...
The fibroblast growth factor and receptor system (FGF/FGFR) mediates cell communication and pattern ...
The form and function of the craniofacial structure critically depend on genetic information. With r...
SUMMARY Apert syndrome is a congenital disorder characterized by severe skull malformations and caus...
Apert syndrome (AS), the most severe form of craniosynostosis, is caused by missense mutations inclu...
Objective: Activating mutations in the fibroblast growth factor receptor-2 (FGFR2) have been shown t...
Apert syndrome is a rare genetic disorder characterized by craniosynostosis, midface retrusion, and ...
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities,...
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities,...
WOS: 000425647900009PubMed ID: 29483804Apert syndrome is an autosomal dominant craniosynostosis synd...
Apert syndrome is an autosomal dominantly inherited disorder caused by missense mutations in fibrobl...