Liu Q - Search Results

1

Molecular investigation in Chinese patients with primary carnitine deficiency.

Zhang Y, Li H, Liu J, Yan H, Liu Q, Wei X, Xi H, Jia Z, Wu L, Wang H. Zhang Y, et al. Among authors: liu j, liu q. Mol Genet Genomic Med. 2019 Sep;7(9):e901. doi: 10.1002/mgg3.901. Epub 2019 Jul 30. Mol Genet Genomic Med. 2019. PMID: 31364285 Free PMC article. Clinical Trial.

2

Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART).

Lv W, Wei X, Guo R, Liu Q, Zheng Y, Chang J, Bai T, Li H, Zhang J, Song Z, Cram DS, Liang D, Wu L. Lv W, et al. Among authors: liu q. Clin Chem. 2015 Jan;61(1):172-81. doi: 10.1373/clinchem.2014.229328. Epub 2014 Nov 6. Clin Chem. 2015. PMID: 25376582

3

[Analysis on the Genotype of 5018 Cases of Thalassemia in Hunan Area].

Liu Q, Jia ZJ, Xi H, Liu J, Peng Y, Wang H. Liu Q, et al. Among authors: liu j. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Dec;27(6):1938-1942. doi: 10.19746/j.cnki.issn.1009-2137.2019.06.037. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019. PMID: 31839063 Chinese.

4

Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome.

He S, Xi H, Chen J, Wang D, Pang J, Hu J, Liu Q, Jia Z, Wang H. He S, et al. Among authors: liu q. Mol Cytogenet. 2020 Feb 11;13:7. doi: 10.1186/s13039-020-0472-y. eCollection 2020. Mol Cytogenet. 2020. PMID: 32071615 Free PMC article.

5

Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.

Liu J, Liu Q, Yang S, Ma N, Pang J, Peng Y, Xi H, Jia Z, Luo Y, Jiang M, Teng Y, Yu W, Li Z, Wang H. Liu J, et al. Among authors: liu q. Mol Genet Genomic Med. 2021 Aug;9(8):e1750. doi: 10.1002/mgg3.1750. Epub 2021 Jul 22. Mol Genet Genomic Med. 2021. PMID: 34293831 Free PMC article. Review.

6

Identification of rare thalassemia variants using third-generation sequencing.

Liu Q, Chen Q, Zhang Z, Peng S, Liu J, Pang J, Jia Z, Xi H, Li J, Chen L, Liu Y, Peng Y. Liu Q, et al. Among authors: liu j, liu y. Front Genet. 2023 Jan 4;13:1076035. doi: 10.3389/fgene.2022.1076035. eCollection 2022. Front Genet. 2023. PMID: 36685902 Free PMC article.

7

Epidemiological Survey of Hemoglobinopathies Based on Next-Generation Sequencing Platform in Hunan Province, China.

Xi H, Liu Q, Xie DH, Zhou X, Tang WL, Tang G, Zeng CY, Wang Q, Nie XH, Peng JP, Gao XY, Wu HL, Zhang HQ, Qiu L, Feng ZH, Wang SY, Zhou SX, He J, Zhou SH, Zhou FQ, Zheng JQ, Wang SY, Chen SP, Zheng ZF, Ma XY, Fang JQ, Liang CB, Wang H. Xi H, et al. Among authors: liu q. Biomed Environ Sci. 2023 Feb 20;36(2):127-134. doi: 10.3967/bes2023.016. Biomed Environ Sci. 2023. PMID: 36861191 Free article.

8

Incidence of cleft lip and palate, and epidemiology of perinatal deaths related to cleft lip and palate in Hunan Province, China, 2016-2020.

Zhou X, Jiang Y, Fang J, Wang H, Xie D, Kuang H, Li T, Liu Q, He J. Zhou X, et al. Among authors: liu q. Sci Rep. 2023 Jun 26;13(1):10304. doi: 10.1038/s41598-023-37436-y. Sci Rep. 2023. PMID: 37365256 Free PMC article.

9

[Expert consensus on clinical genetic counseling of α-thalassemia gene analysis].

Xi H, Liu Q, Liu J, Yu W, Wu X, Chang Q. Xi H, et al. Among authors: liu j, liu q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Jun 10;41(6):669-676. doi: 10.3760/cma.j.cn511374-20240131-00079. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38818550 Chinese.

10

Fetal deaths from birth defects in Hunan Province, China, 2016-2020.

Zhou X, He J, Wang A, Hua X, Li T, Liu Q, Fang J, Jiang Y, Shi Y. Zhou X, et al. Among authors: liu q. Sci Rep. 2024 Jul 2;14(1):15163. doi: 10.1038/s41598-024-65985-3. Sci Rep. 2024. PMID: 38956101 Free PMC article.

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