Xu L - Search Results

1

Non-invasive cell-free fetal DNA testing for aneuploidy: multicenter study of 31 515 singleton pregnancies in southeastern China.

Xu L, Huang H, Lin N, Wang Y, He D, Zhang M, Chen M, Chen L, Lin Y. Xu L, et al. Ultrasound Obstet Gynecol. 2020 Feb;55(2):242-247. doi: 10.1002/uog.20416. Epub 2020 Jan 8. Ultrasound Obstet Gynecol. 2020. PMID: 31364782 Free article.

2

A new β-thalassemia deletion mutation [codon 36 (-C)] observed in a Chinese woman.

Huang H, Xu L, Lin N, Xu J, He D, Li Y, Zheng L, Liu H, Lin Y. Huang H, et al. Among authors: xu l, xu j. Hemoglobin. 2010;34(6):599-603. doi: 10.3109/03630269.2010.526841. Hemoglobin. 2010. PMID: 21077770

3

Quadruplex real-time polymerase chain reaction assay for molecular diagnosis of Y-chromosomal microdeletions.

Guo Q, Lan F, Xu L, Jiang Y, Xiao L, Huang H, Zhou Y. Guo Q, et al. Among authors: xu l. Fertil Steril. 2012 Apr;97(4):864-9. doi: 10.1016/j.fertnstert.2012.01.088. Epub 2012 Jan 23. Fertil Steril. 2012. PMID: 22270555 Free article.

4

[Relationship between gene polymorphism of GABAA receptors gene and childhood autism].

Lu GB, Ou P, Xu LP, Huang HL, Cheng L, Yang SW, Qian QF, Huang Y, Xie YQ, Yu QJ, Wang ZQ, Lin Y. Lu GB, et al. Among authors: xu lp. Zhonghua Yu Fang Yi Xue Za Zhi. 2012 May;46(5):460-4. Zhonghua Yu Fang Yi Xue Za Zhi. 2012. PMID: 22883737 Chinese.

5

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.

Liang D, Lv W, Wang H, Xu L, Liu J, Li H, Hu L, Peng Y, Wu L. Liang D, et al. Among authors: xu l. Prenat Diagn. 2013 May;33(5):409-15. doi: 10.1002/pd.4033. Epub 2013 Jan 9. Prenat Diagn. 2013. PMID: 23299662

6

Molecular spectrum of β-thalassemia in Fujian Province, Southeastern China.

Huang H, Xu L, Lin N, He D, Li Y, Guo D, Wang L, Wang Y, Zhen L, Xu J, Lin Y. Huang H, et al. Among authors: xu l, xu j. Hemoglobin. 2013;37(4):343-50. doi: 10.3109/03630269.2013.792274. Epub 2013 May 20. Hemoglobin. 2013. PMID: 23682686

7

[Molecular epidemiological analysis of α- and β-thalassemia in Fujian province].

Xu LP, Huang HL, Wang Y, Zheng L, Wang LS, Xu JB, Huang XX, Lin Y. Xu LP, et al. Among authors: xu jb. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):403-6. doi: 10.3760/cma.j.issn.1003-9406.2013.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926004 Chinese.

8

A multicenter study of fetal chromosomal abnormalities in Chinese women of advanced maternal age.

Zhu Y, Lu S, Bian X, Wang H, Zhu B, Wang H, Xu Z, Xu L, Yan W, Zeng Y, Chen Z, Tang S, Shen G, Miao Z. Zhu Y, et al. Among authors: xu l, xu z. Taiwan J Obstet Gynecol. 2016 Jun;55(3):379-84. doi: 10.1016/j.tjog.2016.01.002. Taiwan J Obstet Gynecol. 2016. PMID: 27343319 Free article.

9

[Gene Diagnosis and Analysis of Clinical Hematological Phenotype of Thailand Deleted α-Thalassemia 1].

Lin N, Huang HL, Wang Y, Zheng L, Fang XQ, Cai MY, Wang LS, Liu HK, Xu LP, Lin Y. Lin N, et al. Among authors: xu lp. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Aug;24(4):1116-20. doi: 10.7534/j.issn.1009-2137.2016.04.029. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 27531785 Chinese.

10

[Prenatal diagnosis of 22q11 microdeletion syndrome].

Cai M, Huang H, Lin N, Guo N, Wu X, Su L, Xu L. Cai M, et al. Among authors: xu l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):192-195. doi: 10.3760/cma.j.issn.1003-9406.2017.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397216 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

41,275 results

Search Page

Filters