Detalhe da pesquisa
1.
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
Hum Genomics
; 15(1): 44, 2021 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34256850
2.
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.
Am J Med Genet A
; 176(11): 2259-2275, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30194818
3.
A role for CTCF and cohesin in subtelomere chromatin organization, TERRA transcription, and telomere end protection.
EMBO J
; 31(21): 4165-78, 2012 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23010778