Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients

BACKGROUND: Treacher Collins syndrome (TCS) is a rare autosomal dominant or recessive disorder, that involves unique bilateral craniofacial malformations. The phenotypes of TCS are extremely diverse. Interventional surgery can improve hearing loss and facial deformity in TCS patients. METHOD: We rec...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Clin Lab Anal
Main Authors: Zhang, Chuan, An, Lisha, Xue, Huiqin, Hao, Shengju, Yan, Yousheng, Zhang, Qinghua, Jin, Xiaohua, Li, Qian, Zhou, Bingbo, Feng, Xuan, Ma, Panpan, Wang, Xing, Chen, Xue, Chen, Cuixia, Cao, Zongfu, Ma, Xu
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7843273/
https://ncbi.nlm.nih.gov/pubmed/32909271
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23567
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados