Xia Z - Search Results

1

Combination of fluorescence color and melting temperature as a two-dimensional label for homogeneous multiplex PCR detection.

Liao Y, Wang X, Sha C, Xia Z, Huang Q, Li Q. Liao Y, et al. Among authors: xia z. Nucleic Acids Res. 2013 Apr;41(7):e76. doi: 10.1093/nar/gkt004. Epub 2013 Jan 18. Nucleic Acids Res. 2013. PMID: 23335787 Free PMC article.

2

Rapid detection of G6PD mutations by multicolor melting curve analysis.

Xia Z, Chen P, Tang N, Yan T, Zhou Y, Xiao Q, Huang Q, Li Q. Xia Z, et al. Mol Genet Metab. 2016 Sep;119(1-2):168-73. doi: 10.1016/j.ymgme.2016.07.006. Epub 2016 Jul 20. Mol Genet Metab. 2016. PMID: 27495838

3

Carrier screening for spinal muscular atrophy with a simple test based on melting analysis.

Xia Z, Zhou Y, Fu D, Wang Z, Ge Y, Ren J, Guo Q. Xia Z, et al. J Hum Genet. 2019 May;64(5):387-396. doi: 10.1038/s10038-019-0576-6. Epub 2019 Feb 15. J Hum Genet. 2019. PMID: 30765868

4

Rapid screening for Klinefelter syndrome with a simple high-resolution melting assay: a multicenter study.

Fu DM, Zhou YL, Zhao J, Hu P, Xu ZF, Lv SM, Hu JJ, Xia ZM, Guo QW. Fu DM, et al. Asian J Androl. 2018 Jul-Aug;20(4):349-354. doi: 10.4103/aja.aja_15_18. Asian J Androl. 2018. PMID: 29600796 Free PMC article.

5

Comparison of the accuracy of multiplex digital PCR versus multiplex ligation-dependent probe amplification in quantification of the survival of motor neuron genes copy numbers.

Jiang Y, Xia Z, Zhou Y, Lu X, Du X, Guo Q. Jiang Y, et al. Among authors: xia z. Clin Chim Acta. 2024 Jan 15;553:117708. doi: 10.1016/j.cca.2023.117708. Epub 2023 Dec 13. Clin Chim Acta. 2024. PMID: 38097128

6

Clinical Utility of a High-Resolution Melting Test for Screening Numerical Chromosomal Abnormalities in Recurrent Pregnancy Loss.

Zhou Y, Xu W, Jiang Y, Xia Z, Zhang H, Chen X, Wang Z, Ge Y, Guo Q. Zhou Y, et al. Among authors: xia z. J Mol Diagn. 2020 Apr;22(4):523-531. doi: 10.1016/j.jmoldx.2020.01.005. Epub 2020 Apr 9. J Mol Diagn. 2020. PMID: 32279948 Free article.

7

Screening and mutation analysis of hyperphenylalaninemia in newborns from Xiamen, China.

Wang X, He Y, Jiang Y, Feng X, Zhang G, Xia Z, Zhou Y. Wang X, et al. Among authors: xia z. Clin Chim Acta. 2019 Nov;498:161-166. doi: 10.1016/j.cca.2019.08.021. Epub 2019 Aug 22. Clin Chim Acta. 2019. PMID: 31445982

8

Evaluation of strategies for identification of infants with pathogenic glucose-6-phosphate dehydrogenase variants in China.

Xia Z, Wang X, Ye H, Gao C, Zhou X, Chen J, Ge Y, Li J, Zhou Y, Guo Q. Xia Z, et al. Front Genet. 2022 Sep 23;13:844381. doi: 10.3389/fgene.2022.844381. eCollection 2022. Front Genet. 2022. PMID: 36212124 Free PMC article.

9

Development of a low-cost and accurate carrier screening method for spinal muscular atrophy in developing countries.

Jiang Y, Luo Z, Wang W, Lu X, Xia Z, Xie J, Lu M, Wu L, Zhou Y, Guo Q. Jiang Y, et al. Among authors: xia z. Eur J Med Genet. 2024 Apr;68:104921. doi: 10.1016/j.ejmg.2024.104921. Epub 2024 Feb 5. Eur J Med Genet. 2024. PMID: 38325644 Free article.

10

Clinical phenotype, in silico and biomedical analyses, and intervention for an East Asian population-specific c.370G>A (p.G124S) COQ4 mutation in a Chinese family with CoQ10 deficiency-associated Leigh syndrome.

Lu M, Zhou Y, Wang Z, Xia Z, Ren J, Guo Q. Lu M, et al. Among authors: xia z. J Hum Genet. 2019 Apr;64(4):297-304. doi: 10.1038/s10038-019-0563-y. Epub 2019 Jan 18. J Hum Genet. 2019. PMID: 30659264

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