AB107. Study of functional independence of patients with osteogenesis imperfecta

BACKGROUND: Osteogenesis imperfecta (OI) is a genetic bone disorder characterized by fragile bones that break easily. It is a complicated, variable and rare disorder. Its major feature is a fragile skeleton, but many other body systems are also affected. OI is caused by a mutation in a gene that aff...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Nguyen, Thu Ha, Thuy, Linh Tran Thi, Thi, Xuan Bui, Thi, Huong Bui, Do Thi, Hoa, Thanh, Hoa Nguyen Thi, Do Thi, Mo, Thu, Ha Nguyen
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2017
Assuntos:
Birth Defects, Dysmorphology, Skeletal Dysplasia, Craniofacial Anomalies
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641763/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s107
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados