<--- Back to Details
First PageDocument Content
Skull / Syndromes / Congenital disorders / Head and neck / Skeletal system / Craniosynostosis / Craniofacial surgery / Brachycephaly / Apert syndrome / Health / Anatomy / Human anatomy
Date: 2010-09-15 09:40:55
Skull
Syndromes
Congenital disorders
Head and neck
Skeletal system
Craniosynostosis
Craniofacial surgery
Brachycephaly
Apert syndrome
Health
Anatomy
Human anatomy

Pediatr Clin N Am[removed] – 387 Skull deformities

Add to Reading List

Source URL: www.med.unc.edu

Download Document from Source Website

File Size: 1,07 MB

Share Document on Facebook

Similar Documents

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

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

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

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

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

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

Brain phenotypes in two FGFR2 mouse models for Apert syndrome

DocID: 1fzZQ - View Document

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

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

DocID: 1fsy4 - View Document