A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients

OBJECTIVE: Palatal anomalies are one of the identifying features of 22q11.2 deletion syndrome (22q11.2DS) affecting about one third of patients. To identify genetic variants that increase the risk of cleft or palatal anomalies in 22q11.2DS patients, we performed a candidate gene association study in...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Widdershoven, Josine C.C., Bowser, Mark, Sheridan, Molly B., McDonald-McGinn, Donna M., Zackai, Elaine H., Solot, Cynthia B., Kirschner, Richard E., Beemer, Frits A., Morrow, Bernice E., Devoto, Marcella, Emanuel, Beverly S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4098838/
https://ncbi.nlm.nih.gov/pubmed/23121717
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijporl.2012.10.009
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados