<--- Back to Details
First PageDocument Content
Crouzon syndrome / Micrognathism / DiGeorge syndrome / Hemifacial microsomia / Goldenhar syndrome / Pierre Robin syndrome / Stickler syndrome / Apert syndrome / Cleft lip and palate / Health / Syndromes / Treacher Collins syndrome
Date: 2010-12-08 18:33:35
Crouzon syndrome
Micrognathism
DiGeorge syndrome
Hemifacial microsomia
Goldenhar syndrome
Pierre Robin syndrome
Stickler syndrome
Apert syndrome
Cleft lip and palate
Health
Syndromes
Treacher Collins syndrome

COMMON OTOLARYNGOLOGICAL CONGENITAL ABNORMALITIES

Add to Reading List

Source URL: www.utmb.edu

Download Document from Source Website

File Size: 949,23 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