当前位置: X-MOL 学术Clin. Dysmorphol. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Mild presentation of the congenital variant Rett syndrome in a Pakistani male: expanding the phenotype of the forkhead box protein G1 spectrum.
Clinical Dysmorphology ( IF 0.7 ) Pub Date : 2019-10-03 , DOI: 10.1097/mcd.0000000000000302
Aleena Arij Khan 1 , Salman Kirmani
Affiliation  



中文翻译:

巴基斯坦男性中先天性变种Rett综合征的轻微表现:扩大了叉头盒蛋白G1谱的表型。

更新日期:2019-11-01
down
wechat
bug