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Developing and validating noninvasive prenatal testing for de novo autosomal dominant monogenic diseases in Vietnam.
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: thi ha tm.
Per Med. 2023 Nov;20(6):467-475. doi: 10.2217/pme-2023-0105. Epub 2023 Nov 8.
Per Med. 2023.
PMID: 37937420
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The genetic landscape of chromosomal aberrations in 3776 Vietnamese fetuses with clinical anomalies during pregnancy.
Tran DC, Phan MN, Dao HT, Nguyen HL, Nguyen DA, Le QT, Hoang DT, Tran NT, Thi Ha TM, Dinh TL, Nguyen CC, Thi Doan KP, Thi Luong LA, Vo TS, Nhat Trinh TH, Nguyen VT, Vo PN, Nguyen YN, Dinh MA, Doan PL, Do TT, Nguyen QT, Truong DK, Nguyen HN, Phan MD, Tang HS, Giang H.
Tran DC, et al. Among authors: thi ha tm.
Per Med. 2024 Apr 4. doi: 10.2217/pme-2023-0113. Online ahead of print.
Per Med. 2024.
PMID: 38573622
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