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.)
Dual genetic diagnoses: neurofibromatosis type 1 and KBG syndrome.
Clinical Dysmorphology ( IF 0.4 ) Pub Date : 2019-10-01 , DOI: 10.1097/mcd.0000000000000296
Paola Cianci 1 , Laura Pezzoli 2 , Silvia Maitz 3 , Massimo Agosti 1 , Maria Iascone 2 , Angelo Selicorni 4
Affiliation  



中文翻译:

双重遗传诊断:1型神经纤维瘤病和KBG综合征。

更新日期:2019-11-01
down
wechat
bug