Detalhe da pesquisa
1.
Integrative overview of IFITMs family based on Bioinformatics analysis.
Intractable Rare Dis Res
; 10(3): 165-172, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-34466338
2.
Comprehensive bioinformatic analysis of Wnt1 and Wnt1-associated diseases.
Intractable Rare Dis Res
; 9(1): 14-22, 2020 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32201670
3.
Health assessment of patients with achondroplasia, pseudoachondroplasia, and rickets based on 3D non-linear diagnostics.
Intractable Rare Dis Res
; 9(1): 35-39, 2020 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32201673
4.
Splice receptor-site mutation c.697-2A>G of the COL1A1 gene in a Chinese family with osteogenesis imperfecta.
Intractable Rare Dis Res
; 8(2): 150-153, 2019 May.
Artigo
Inglês
| MEDLINE | ID: mdl-31218168