Liu L - Search Results

1

[Genetic Analysis, Prenatal Diagnosis and Preimplantation Genetic Diagnosis of Taiwanese Deletion β-Thalassemia].

DU L, Qin DQ, Liu L, Lu J, Yao CZ, Huang HJ, Wang JC. DU L, et al. Among authors: liu l. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Oct;27(5):1585-1591. doi: 10.19746/j.cnki.issn.1009-2137.2019.05.034. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019. PMID: 31607316 Chinese.

2

Characterisation of two unusual cases of haemoglobin Bart's hydrops foetalis caused by -^SEA and large novel α-globin gene cluster deletions.

Wang Y, Xiong Y, Liu C, Lu J, Wang J, Qin D, Liu L, Wu J, Zhao X, Fang L, Du L, Yin A. Wang Y, et al. Among authors: liu l, liu c. J Int Med Res. 2021 Feb;49(2):300060521993642. doi: 10.1177/0300060521993642. J Int Med Res. 2021. PMID: 33596700 Free PMC article.

3

[Differential Diagnosis of Three Commonest Deletion β-Thalassemia in Chinese].

Wang JC, Yao CZ, Huang YL, Liu L, Yuan TL, Qin DQ. Wang JC, et al. Among authors: liu l. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Aug;29(4):1247-1250. doi: 10.19746/j.cnki.issn.1009-2137.2021.04.035. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021. PMID: 34362510 Chinese.

4

Genetic and phenotypic analysis of a rare asymptomatic case of a homozygous Chinese ^Gγ⁺(^Aγδβ)⁰-thalassemia deletion in a Chinese family.

Du L, Qin D, Wang J, Yu L, Yao C, Liu L, Zhang Y, Hu T, Yuan T, Liang J, Yin A. Du L, et al. Among authors: liu l. Clin Biochem. 2020 Feb;76:11-16. doi: 10.1016/j.clinbiochem.2019.11.003. Epub 2019 Nov 22. Clin Biochem. 2020. PMID: 31765637

5

[Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese].

Liu L, Jiang WY, Xu SY, Chen J, Chen LM, Tian QH, Wang JC. Liu L, et al. Zhonghua Xue Ye Xue Za Zhi. 2013 Jul;34(7):595-9. doi: 10.3760/cma.j.issn.0253-2727.2013.07.008. Zhonghua Xue Ye Xue Za Zhi. 2013. PMID: 23906453 Chinese.

6

[Analysis of clinical feature and genetic basis of a rare case with Olmsted syndrome].

Lu J, Hu R, Liu L, Ding H. Lu J, et al. Among authors: liu l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jul 10;38(7):674-677. doi: 10.3760/cma.j.cn511374-20200811-00597. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34247376 Chinese.

7

Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China.

Liu C, Zhang X, Wang J, Zhang Y, Wang A, Lu J, Huang Y, Liu S, Wu J, Du L, Yang J, Ding H, Liu L, Zhao X, Yin A. Liu C, et al. Among authors: liu l, liu s. Mol Cytogenet. 2019 Feb 18;12:7. doi: 10.1186/s13039-019-0420-x. eCollection 2019. Mol Cytogenet. 2019. PMID: 30820248 Free PMC article.

8

Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.

Liu C, Huang Y, Zhang Y, Ding H, Yu L, Wang A, Wang Y, Zeng Y, Liu L, Liu Y, Qi Y, Li F, Wu J, Du L, Mai F, Zhang Q, Wang X, Yin A. Liu C, et al. Among authors: liu y, liu l. Int J Pediatr Otorhinolaryngol. 2022 Oct;161:111258. doi: 10.1016/j.ijporl.2022.111258. Epub 2022 Jul 31. Int J Pediatr Otorhinolaryngol. 2022. PMID: 35939872

9

Development of a community-based hearing loss prevention and control service model in Guangdong, China.

Liu C, Wang A, Huang Y, Zhang Y, Ding H, Wu J, Du L, Yang J, Mai F, Zeng Y, Liu L, Zhao X, Zhang C, Yin A. Liu C, et al. Among authors: liu l. BMC Public Health. 2019 Nov 29;19(1):1601. doi: 10.1186/s12889-019-7910-y. BMC Public Health. 2019. PMID: 31783833 Free PMC article.

10

A Multidisciplinary Approach in Prenatal Diagnosis of TSC With Cardiac Rhabdomyoma as the Initial Symptom.

Qi Y, Ding H, Huang Y, Zeng Y, Yu L, Liu L, Zhang Y, Yin A. Qi Y, et al. Among authors: liu l. Front Pediatr. 2021 Aug 27;9:628238. doi: 10.3389/fped.2021.628238. eCollection 2021. Front Pediatr. 2021. PMID: 34513752 Free PMC article.

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