Velopharyngeal Anatomy in 22q11.2 Deletion Syndrome: A Three-Dimensional Cephalometric Analysis

OBJECTIVE: 22q11.2 deletion syndrome is the most common genetic cause of velopharyngeal dysfunction (VPD). Magnetic resonance imaging (MRI) is a promising method for noninvasive, three-dimensional (3D) assessment of velopharyngeal (VP) anatomy. The purpose of this study was to assess VP structure in...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ruotolo, Rachel A., Veitia, Nestor A., Corbin, Aaron, McDonough, Joseph, Solot, Cynthia B., McDonald-McGinn, Donna, Zackai, Elaine H., Emanuel, Beverly S., Cnaan, Avital, LaRossa, Don, Arens, Raanan, Kirschner, Richard E.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2006
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2813062/
https://ncbi.nlm.nih.gov/pubmed/16854203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1597/04-193R.1
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg