Detalhe da pesquisa
1.
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
Genet Med
; 26(7): 101126, 2024 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38529886
2.
Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qterâq21.11::p23.3âqter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature.
Am J Med Genet A
; 182(11): 2680-2684, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32803851
3.
Computational approaches for discovering significant microRNAs, microRNA-mRNA regulatory pathways, and therapeutic protein targets in endometrial cancer.
Front Genet
; 13: 1105173, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36704357
4.
Novel mutation points to a hot spot in CDKN1C causing Silver-Russell syndrome.
Clin Epigenetics
; 12(1): 152, 2020 10 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33076988