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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2012 1
2014 1
2015 1
2016 1
2018 4
2019 1
2020 2
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2022 4
2023 2
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Page 1
Genetic analyses of Vietnamese patients with oculocutaneous albinism.
Thuong MTH, Anh LTL, Nhung VP, Ngoc TTB, Lan HT, Phuong DK, Ha NH, Van Hai N, Ton ND. Thuong MTH, et al. Among authors: van hai n. J Clin Lab Anal. 2022 Sep;36(9):e24625. doi: 10.1002/jcla.24625. Epub 2022 Jul 23. J Clin Lab Anal. 2022. PMID: 35870188 Free PMC article.
Novel and very rare causative variants in the COL7A1 gene of Vietnamese patients with recessive dystrophic epidermolysis bullosa revealed by whole-exome sequencing.
Ma THT, Luong TLA, Hoang TL, Nguyen TTH, Vu TH, Tran VK, Nguyen DB, Trieu TS, Nguyen HH, Nong VH, Nguyen DT. Ma THT, et al. Among authors: nong vh. Mol Genet Genomic Med. 2021 Aug;9(8):e1748. doi: 10.1002/mgg3.1748. Epub 2021 Jul 19. Mol Genet Genomic Med. 2021. PMID: 34286919 Free PMC article.
The paternal and maternal genetic history of Vietnamese populations.
Macholdt E, Arias L, Duong NT, Ton ND, Van Phong N, Schröder R, Pakendorf B, Van Hai N, Stoneking M. Macholdt E, et al. Among authors: van hai n. Eur J Hum Genet. 2020 May;28(5):636-645. doi: 10.1038/s41431-019-0557-4. Epub 2019 Dec 11. Eur J Hum Genet. 2020. PMID: 31827276 Free PMC article.
Whole Genome Sequencing of a Vietnamese Family from a Dioxin Contamination Hotspot Reveals Novel Variants in the Son with Undiagnosed Intellectual Disability.
Nguyen DT, Nguyen HH, Nguyen TD, Nguyen TTH, Nakano K, Maejima K, Sasaki-Oku A, Nguyen VB, Nguyen DB, Le BQ, Wong JH, Tsunoda T, Nakagawa H, Fujimoto A, Nong VH. Nguyen DT, et al. Among authors: nong vh. Int J Environ Res Public Health. 2018 Nov 23;15(12):2629. doi: 10.3390/ijerph15122629. Int J Environ Res Public Health. 2018. PMID: 30477169 Free PMC article.
18 results