Preselection of cases through expert clinical and radiological review significantly increases mutation detection rate in multiple epiphyseal dysplasia

Skeletal dysplasias are difficult to diagnose for the nonexpert. In a previous study of patients with multiple epiphyseal dysplasia (MED), we identified cartilage oligomeric matrix protein (COMP) mutations in only 36% of cases and suspected that the low-mutation detection rate was partially due to m...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Zankl, Andreas, Jackson, Gail C, Crettol, Laureane Mittaz, Taylor, Jacky, Elles, Rob, Mortier, Geert R, Spranger, Jurgen, Zabel, Bernhard, Unger, Sheila, Le Merrer, Martine, Cormier-Daire, Valerie, Hall, Christine M, Wright, Michael J, Bonafe, Luisa, Superti-Furga, Andrea, Briggs, Michael D
Formato: Artigo
Idioma:English
Publicado em: 2006
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2670452/
https://ncbi.nlm.nih.gov/pubmed/17133256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201744
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Internet

https://ncbi.nlm.nih.gov/pmc/articles/PMC2670452/
https://ncbi.nlm.nih.gov/pubmed/17133256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201744

Registos relacionados