Works matching AU Ta, Thanh-Van
Results: 19
Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.
- Published in:
- Haemophilia, 2019, v. 25, n. 4, p. e274, doi. 10.1111/hae.13738
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- Publication type:
- Article
In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2263
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- Publication type:
- Article
Family based and case–control designs reveal an association of TFAP2A in nonsyndromic cleft lip only among Vietnamese population.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 9, p. 1, doi. 10.1002/mgg3.1754
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- Article
Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1648
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- Article
Quality of Life in Vietnamese Gastric Cancer Patients.
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- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/7167065
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- Publication type:
- Article
The Impact of Vaccination on COVID-19 Outcomes in Vietnam.
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- Diagnostics (2075-4418), 2024, v. 14, n. 24, p. 2850, doi. 10.3390/diagnostics14242850
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- Publication type:
- Article
BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome.
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- Genes, 2022, v. 13, n. 2, p. 268, doi. 10.3390/genes13020268
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- Publication type:
- Article
Mutation spectrum of CYP21A2 and correlation between genotype - phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency.
- Published in:
- 2013
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- Publication type:
- Abstract
Analysis of the cause of recurrent pregnancy loss in Vietnam: A cross-sectional study.
- Published in:
- Health Care for Women International, 2018, v. 39, n. 4, p. 463, doi. 10.1080/07399332.2017.1391264
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- Publication type:
- Article
Breast Cancer Survival Defined by Biological Receptor and Menopausal Status in Vietnamese Women.
- Published in:
- 2019
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- Publication type:
- journal article
Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report.
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- 2023
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- Publication type:
- Case Study
Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 variants.
- Published in:
- 2019
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- Publication type:
- Letter
Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia.
- Published in:
- PLoS ONE, 2022, v. 17, n. 12, p. 1, doi. 10.1371/journal.pone.0278539
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- Publication type:
- Article
Polymorphism of MUC1 Gene in Vietnamese Gastric Cancer Patients: A Multicenter Case–Control Study.
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- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.694977
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- Publication type:
- Article
Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.
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- Anemia (20901267), 2022, p. 1, doi. 10.1155/2022/2653089
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- Publication type:
- Article
Nutritional Status, Refeeding Syndrome and Some Associated Factors of Patients at COVID-19 Hospital in Vietnam.
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- Nutrients, 2023, v. 15, n. 7, p. 1760, doi. 10.3390/nu15071760
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- Publication type:
- Article
Hyperornithinemia–Hyperammonemia–Homocitrullinuria Syndrome in Vietnamese Patients.
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- 2024
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- Publication type:
- Case Study
A case of self‐improving collodion ichthyosis in Vietnam.
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- Pediatric Dermatology, 2020, v. 37, n. 3, p. 574, doi. 10.1111/pde.14128
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- Publication type:
- Article
Fructose 1,6-Bisphosphate Aldolase Is a Heparin-Binding Protein.
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- Journal of Biochemistry, 1999, v. 125, n. 3, p. 554
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- Publication type:
- Article