Detalhe da pesquisa
1.
[Genetic analysis of a child with Complex cortical dysplasia with other brain malformations type 6 due to a p.M73V variant of TUBB gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(12): 1541-1545, 2023 Dec 10.
Artigo
em Zh
| MEDLINE | ID: mdl-37994139
2.
Charge Transfer Gap Tuning via Structural Distortion in Monolayer 1T-NbSe2.
Nano Lett
; 21(16): 7005-7011, 2021 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34350759
3.
Novel IARS1 variants cause syndromic developmental disorder with epilepsy in a Chinese patient and the literature review.
Mol Genet Genomic Med
; 12(1): e2326, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38014478
4.
Correlation of TGF-ß signaling pathway gene polymorphisms with unexplained recurrent spontaneous abortion.
Medicine (Baltimore)
; 102(43): e35697, 2023 Oct 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37904417
5.
Prenatal diagnosis in a fetuses with a clenched hands, overlapping fingers, and clubfoot due to MED12 deficiency in three affected siblings: A case report.
Front Genet
; 14: 1037345, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37501721
6.
Realization of AlSb in the Double-Layer Honeycomb Structure: A Robust Class of Two-Dimensional Material.
ACS Nano
; 15(5): 8184-8191, 2021 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33723991