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Massively parallel sequencing uncovered disease-associated variant spectra of glucose-6-phosphate dehydrogenase deficiency, phenylketonuria and galactosemia in Vietnamese pregnant women.
Nguyen TT, Le QT, Hoang DT, Du Nguyen H, Ha TMT, Nguyen MB, Ta TT, Tran NT, Trinh THN, Doan KPT, Lam DT, Tran STT, Nguyen TX, Le HT, Ha VT, Nguyen MH, Le BK, Duong ML, Pham TH, Tran AT, Phan XLT, Huynh TL, Nguyen LT, Vo TB, Le DN, Tran NNT, Tran QNT, Van YT, Huynh BT, Nguyen TT, Dao TT, Nguyen LPT, Vo TG, Do TT, Truong DK, Tang HS, Phan MD, Nguyen HN, Giang H. Nguyen TT, et al. Among authors: le bk, le dn, le ht, le qt. Mol Genet Genomic Med. 2022 Jul;10(7):e1959. doi: 10.1002/mgg3.1959. Epub 2022 May 3. Mol Genet Genomic Med. 2022. PMID: 35502621 Free PMC article.
Developing and validating noninvasive prenatal testing for de novo autosomal dominant monogenic diseases in Vietnam.
Nguyen NY, Lu YT, Nguyen DA, Nguyen CC, Dinh LT, Tran MT, Tran DC, Luong LT, Doan KP, Huy Nguyen VQ, Thi Ha TM, Truong LT, Tran NT, Cao PT, Tran VT, Nhut Trinh TH, Le QT, Nguyen VT, Hoang DT, Vo ST, Nguyen MB, Bui CT, Tran ST, Lam DT, Le HT, Nguyen MB, Ho VT, Nguyen MT, Doan PL, Tran KT, Tran HT, Tran UV, Dinh AM, Nguyen TT, Do TT, Truong DK, Phan MD, Nguyen HN, Tang HS, Giang H. Nguyen NY, et al. Among authors: le ht, le qt. Per Med. 2023 Sep;20(5):425-433. doi: 10.2217/pme-2023-0076. Epub 2023 Aug 25. Per Med. 2023. PMID: 37623819
De novo variants of dominant monogenic disorders in Vietnam detected by a noninvasive prenatal test: a case series.
Tran NT, Vo ST, Nguyen DA, Nguyen CC, Dinh LT, Tran MT, Tran DC, Luong LT, Doan KP, Huy Nguyen VQ, Thi Ha TM, Truong LT, Cao PT, Tran VT, Nhut Trinh TH, Le QT, Nguyen VT, Hoang DT, Nguyen MB, Bui CT, Tran ST, Lam DT, Le HT, Nguyen MB, Ho VT, Nguyen MT, Dao TT, Nguyen PM, Nguyen TL, Ha NP, Lu YT, Do TT, Truong DK, Phan MD, Nguyen HN, Giang H, Tang HS. Tran NT, et al. Among authors: le ht, le qt. Per Med. 2023 Nov;20(6):467-475. doi: 10.2217/pme-2023-0105. Epub 2023 Nov 8. Per Med. 2023. PMID: 37937420
564 results