Weng XJ - Search Results

1

Diagnostic Accuracy of Prenatal Fetal Ultrasound to Detect Cleft Palate in High-Risk Fetuses: A Systematic Review and Meta-Analysis.

Lai GP, Weng XJ, Wang M, Tao ZF, Liao FH. Lai GP, et al. Among authors: weng xj. J Ultrasound Med. 2022 Mar;41(3):605-614. doi: 10.1002/jum.15736. Epub 2021 Apr 27. J Ultrasound Med. 2022. PMID: 33904621

2

Rapid diagnosis of aneuploidy using segmental duplication quantitative fluorescent PCR.

Kong X, Li L, Sun L, Fu K, Long J, Weng X, Ye X, Liu X, Wang B, Yan S, Ye H, Fan Z. Kong X, et al. PLoS One. 2014 Mar 13;9(3):e88932. doi: 10.1371/journal.pone.0088932. eCollection 2014. PLoS One. 2014. PMID: 24625828 Free PMC article.

3

Molecular diagnosis of sex chromosome mosaics in fetal amniotic cells.

Fan Z, Weng X, Pan Z, Fan Q, Long J, Lin G, Yang Q, Sun L. Fan Z, et al. Medicine (Baltimore). 2021 Jun 25;100(25):e26331. doi: 10.1097/MD.0000000000026331. Medicine (Baltimore). 2021. PMID: 34160397 Free PMC article.

4

Serum multiple cytokines for the prediction of spontaneous preterm birth in asymptomatic women: A nested case-control study.

Huang L, Hou Q, Huang Y, Ye J, Huang S, Tian J, Tang R, Liu C, Long Y, Qin X, Weng X, Huang Y, Li M, Yang X, Mo Z. Huang L, et al. Cytokine. 2019 May;117:91-97. doi: 10.1016/j.cyto.2019.02.007. Epub 2019 Mar 1. Cytokine. 2019. PMID: 30831445

5

STARD-rapid screening for the 6 most common G6PD gene mutations in the Chinese population using the amplification refractory mutation system combined with melting curve analysis.

Fan Z, Weng X, Huang G, Pan Z, Long Z, Fan Q, Tang W, Fang L, Long J, Hu T, Huang Y, Sun L. Fan Z, et al. Medicine (Baltimore). 2018 Apr;97(17):e0426. doi: 10.1097/MD.0000000000010426. Medicine (Baltimore). 2018. PMID: 29702993 Free PMC article.

6

Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, X, and Y using segmental duplication quantitative fluorescent PCR (SD-QF-PCR).

Sun L, Fan Z, Long J, Weng X, Tang W, Pang W. Sun L, et al. Gene. 2017 Sep 5;627:72-78. doi: 10.1016/j.gene.2017.06.014. Epub 2017 Jun 9. Gene. 2017. PMID: 28603073

7

Rapid detection of Down's syndrome using quantitative real-time PCR (qPCR) targeting segmental duplications on chromosomes 21 and 11.

Sun L, Fan Z, Weng X, Ye X, Long J, Fu K, Yan S, Wang B, Zhuo Y, Liu X, Lao K. Sun L, et al. Gene. 2014 Dec 1;552(2):272-6. doi: 10.1016/j.gene.2014.09.044. Epub 2014 Sep 23. Gene. 2014. PMID: 25256276

8

Rapid diagnosis of aneuploidy in chromosomes 13, 18, 21, X and Y by quantitative fluorescence-PCR combined with short tandem repeat and fluorescence-labeled homologous gene quantitative‑PCR using 4-color fluorescently labeled universal primers.

Long J, Ye X, Weng X, Fu K, Sun L, Pang W. Long J, et al. Mol Med Rep. 2013 Nov;8(5):1601-5. doi: 10.3892/mmr.2013.1678. Epub 2013 Sep 13. Mol Med Rep. 2013. PMID: 24042581

9

Identification of Three Types of α-Thalassemia Deletion, -α^21.9, -α^2.4, and - -^THAI, and Their Frequencies, in One Family in the Population of Southern Guangxi Zhuang Autonomous Region, People's Republic of China.

Pang W, Long J, Weng X, Fan Q, Sun L, Pan Z, Fan Z. Pang W, et al. Hemoglobin. 2018 Jan;42(1):37-42. doi: 10.1080/03630269.2018.1428618. Epub 2018 Feb 15. Hemoglobin. 2018. PMID: 29447013

10

Detection of three common α-thalassemia in non-deletion types and six common thalassemia in deletion types by QF-PCR.

Long J, Ye X, Lao K, Pang W, Weng X, Fu K, Yan S, Sun L. Long J, et al. Clin Biochem. 2013 Dec;46(18):1860-4. doi: 10.1016/j.clinbiochem.2013.09.013. Epub 2013 Sep 23. Clin Biochem. 2013. PMID: 24070774

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