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.)
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion.
Clinical Dysmorphology ( IF 0.4 ) Pub Date : 2020-07-01 , DOI: 10.1097/mcd.0000000000000325
Ingrid Anne Mandy Schierz 1 , Gregorio Serra 1 , Vincenzo Antona 1 , Ivana Persico 2 , Giovanni Corsello 1 , Ettore Piro 1
Affiliation  



中文翻译:

由于CRLF1缺失的复合杂合性,导致了Crisponi综合征的婴儿发育概况。

更新日期:2020-05-19
down
wechat
bug