Search details
1.
Shift from a Zero-COVID strategy to a New-normal strategy for controlling SARS-COV-2 infections in Vietnam.
Epidemiol Infect
; 151: e117, 2023 07 04.
Article
in English
| MEDLINE | ID: mdl-37401482
2.
A Novel Nonsense Mutation c.374C>G in CYP21A2 Gene of a Vietnamese Patient with Congenital Adrenal Hyperplasia.
Adv Exp Med Biol
; 1292: 27-35, 2020.
Article
in English
| MEDLINE | ID: mdl-30838541
3.
Variation of Mitochondrial DNA HV1 AND HV2 of the Vietnamese Population.
Adv Exp Med Biol
; 1292: 37-63, 2020.
Article
in English
| MEDLINE | ID: mdl-30838542
4.
A case of self-improving collodion ichthyosis in Vietnam.
Pediatr Dermatol
; 37(3): 574-575, 2020 May.
Article
in English
| MEDLINE | ID: mdl-32105361
5.
Acromesomelic dysplasia Maroteaux-type in patients from Vietnam.
Am J Med Genet A
; 179(8): 1420-1422, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31077548
6.
Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGS.
J Hum Genet
; 62(5): 531-537, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-28100912
7.
Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.
Haemophilia
; 25(4): e274-e277, 2019 Jul.
Article
in English
| MEDLINE | ID: mdl-30913330
8.
Application of short tandem repeats (STRs) in the preimplantation genetic diagnosis (PGD) of α-thalassemia.
Taiwan J Obstet Gynecol
; 63(3): 375-380, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38802201
9.
A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients.
Front Pediatr
; 12: 1165492, 2024.
Article
in English
| MEDLINE | ID: mdl-38415210
10.
Exon deletion patterns of the dystrophin gene in 82 Vietnamese Duchenne/Becker muscular dystrophy patients.
J Neurogenet
; 27(4): 170-5, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-24099565
11.
Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing.
Front Pediatr
; 11: 1128716, 2023.
Article
in English
| MEDLINE | ID: mdl-36873642
12.
Targeted next-generation sequencing determined a novel SGCG variant that is associated with limb-girdle muscular dystrophy type 2C: A case report.
Clin Case Rep
; 11(3): e7025, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-36992678
13.
Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease.
Front Genet
; 14: 1248338, 2023.
Article
in English
| MEDLINE | ID: mdl-37900180
14.
The first Vietnamese patient who presented late onset of pantothenate kinase-associated neurodegeneration diagnosed by whole exome sequencing: A case report.
Medicine (Baltimore)
; 102(43): e34853, 2023 Oct 27.
Article
in English
| MEDLINE | ID: mdl-37904482
15.
Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.
Front Genet
; 14: 1183663, 2023.
Article
in English
| MEDLINE | ID: mdl-37388928
16.
In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.
Mol Genet Genomic Med
; 11(12): e2263, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37547970
17.
Mutation spectrum of retinoblastoma patients in Vietnam.
Mol Genet Genomic Med
; 11(11): e2244, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-37548407
18.
Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia.
PLoS One
; 17(12): e0278539, 2022.
Article
in English
| MEDLINE | ID: mdl-36476827
19.
Preimplantation genetic testing (PGT) for hemophilia A: Experience from one center.
Taiwan J Obstet Gynecol
; 61(6): 1009-1014, 2022 Nov.
Article
in English
| MEDLINE | ID: mdl-36427965
20.
Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency.
Taiwan J Obstet Gynecol
; 61(1): 153-156, 2022 Jan.
Article
in English
| MEDLINE | ID: mdl-35181030