Search details
1.
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.
Am J Hum Genet
; 2024 May 28.
Article
in English
| MEDLINE | ID: mdl-38815585
2.
The molecular genetics of nELAVL in brain development and disease.
Eur J Hum Genet
; 31(11): 1209-1217, 2023 11.
Article
in English
| MEDLINE | ID: mdl-37697079
Results
1 -
2
de 2
1
Next >
>>