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In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome.
Published in:
Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2263
By:
- Pham, Hung Manh;
- Nguyen, Duy Phuong;
- Ta, Thanh Dat;
- Le, Thi Phuong;
- Phan, Phong Hai;
- Trinh, Hoai An;
- Tran, Tuan Viet;
- Luong, Thi Lan Anh;
- Nguyen, Ha Minh;
- Bui, The‐Hung;
- Tran, Thinh Huy;
- Ta, Thanh Van;
- Tran, Van‐Khanh
Publication type:
Article
Mutation spectrum of retinoblastoma patients in Vietnam.
Published in:
Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 11, p. 1, doi. 10.1002/mgg3.2244
By:
- Linh, Dao Nguyen Ha;
- Van Huy, Nguyen;
- Nguyen, Phuoc‐Dung;
- Le Thi, Phuong;
- Tuan, Hoang Anh;
- Van Nguyen, Trong;
- Tran, Thu Ha;
- Tran, Hai Anh;
- Ta, Thanh Dat;
- Pham, Tuan L. A.;
- Bui, The‐Hung;
- Tran, Thinh Huy;
- Van Ta, Thanh;
- Tran, Van‐Khanh
Publication type:
Article
Acromesomelic dysplasia Maroteaux‐type in patients from Vietnam.
Published in:
American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1420, doi. 10.1002/ajmg.a.61192
By:
- Tran, Thinh Huy;
- Cao, My Ha;
- Luong, Long Hoang;
- Le, Phuong Thi;
- Vu, Dung Chi;
- Ta, Thanh Dat;
- Bui, The‐Hung;
- Nguyen, Duc Hinh;
- Van Ta, Thanh;
- Tran, Van Khanh
Publication type:
Article
Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report.
Published in:
2023
By:
- Tran, Nam‐Chung;
- Nguyen, Tuan Anh;
- Ta, Thanh Dat;
- Tran, Thinh Huy;
- Nguyen, Phuoc‐Dung;
- Vu, Chi Dung;
- Nguyen, Van‐Hung;
- Bui, The‐Hung;
- Ta, Thanh Van;
- Tran, Van Khanh
Publication type:
Case Study
Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease.
Published in:
Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1248338
By:
- Nam Chung Tran;
- Nguyen Thi Kim Lien;
- Thanh Dat Ta;
- Van Hung Nguyen;
- Huy Thinh Tran;
- Nguyen Van Tung;
- Nguyen Thi Xuan;
- Nguyen Huy Hoang;
- Van Khanh Tran
Publication type:
Article
Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.
Published in:
Anemia (20901267), 2022, p. 1, doi. 10.1155/2022/2653089
By:
- Ngo, Thi Thao;
- Tran, Thinh Huy;
- Ta, Thanh Dat;
- Le, Thi Phuong;
- Nguyen, Phuoc Dung;
- Tran, Mai Anh;
- Bui, The-Hung;
- Ta, Thanh Van;
- Tran, Van Khanh
Publication type:
Article

Found: 6

In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome.

Mutation spectrum of retinoblastoma patients in Vietnam.

Acromesomelic dysplasia Maroteaux‐type in patients from Vietnam.

Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report.

Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease.

Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.