Detalhe da pesquisa
1.
Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes.
Int Ophthalmol
; 41(1): 121-134, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32869108
2.
A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.
Mol Vis
; 22: 342-51, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27122965
3.
Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel.
Cureus
; 15(5): e39067, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37323311
4.
Genotypic and phenotypic profiles of EYS gene-related retinitis pigmentosa: a retrospective study.
Sci Rep
; 12(1): 21494, 2022 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36513702
5.
Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridia.
Mol Vis
; 17: 1305-9, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21633710
6.
Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene.
PeerJ
; 7: e6501, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30828495
7.
Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.
Invest Ophthalmol Vis Sci
; 58(4): 2413-2420, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28453600
8.
Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes.
Invest Ophthalmol Vis Sci
; 55(4): 2259-68, 2014 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-24618324
9.
Mutations in the XLRS1 gene in Thai families with X-linked juvenile retinoschisis.
Jpn J Ophthalmol
; 54(1): 89-93, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20151283
10.
Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.
Ophthalmic Genet
; 29(3): 139-44, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18766995