Detalhe da pesquisa
1.
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy.
Genet Med
; 21(4): 1008-1014, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30166628
2.
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases.
Clin Genet
; 94(1): 141-152, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29574747
3.
Homozygous FIBP nonsense variant responsible of syndromic overgrowth, with overgrowth, macrocephaly, retinal coloboma and learning disabilities.
Clin Genet
; 89(5): e1-4, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26660953