Detalhe da pesquisa
1.
Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation.
Hum Mol Genet
; 32(9): 1439-1456, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36458887
2.
Reprogramming of the histone H3.3 landscape in the early mouse embryo.
Nat Struct Mol Biol
; 28(1): 38-49, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33169018