<--- Back to Details
First PageDocument Content
Congenital disorders / Rare diseases / Skull / Craniosynostosis / Crouzon syndrome / Apert syndrome / Pfeiffer syndrome / Muenke syndrome / Carpenter syndrome / Health / Syndromes / Genodermatoses
Date: 2008-12-06 10:39:14
Congenital disorders
Rare diseases
Skull
Craniosynostosis
Crouzon syndrome
Apert syndrome
Pfeiffer syndrome
Muenke syndrome
Carpenter syndrome
Health
Syndromes
Genodermatoses

Add to Reading List

Source URL: www.ameriface.org

Download Document from Source Website

File Size: 125,39 KB

Share Document on Facebook

Similar Documents

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

DocID: 1lqdu - View Document

FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Neus Martı´nez-Abadı´as1, Yann Heuze´1, Yingli Wang2, Ethylin Wang Jab

DocID: 1krlW - View Document

Anatomy / Genodermatoses / Tyrosine kinase receptors / Fibroblast growth factor receptor 2 / Apert syndrome / Crouzon syndrome / Craniosynostosis / Fibroblast growth factor / Neurocranium / Health / Biology / Syndromes

FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Neus Martı´nez-Abadı´as1, Yann Heuze´1, Yingli Wang2, Ethylin Wang Jab

DocID: 1gf6m - View Document

Biology / Genodermatoses / Apert syndrome / Craniosynostosis / Fibroblast growth factor receptor 2 / Corpus callosum / Suture / Ventriculomegaly / Health / Anatomy / Syndromes

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

DocID: 1fzZQ - View Document

Syndromes / Congenital disorders / Skull / Genodermatoses / Craniosynostosis / Apert syndrome / Fibroblast growth factor receptor 2 / Saethre-Chotzen syndrome / Suture / Health / Anatomy / Human anatomy

DEVELOPMENTAL DYNAMICS 239:3058–3071, 2010 a PATTERNS & PHENOTYPES

DocID: 1fsy4 - View Document