Yu L - Search Results

1

Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study.

Huang Y, Liu C, Ding H, Wang Y, Yu L, Guo F, Li F, Shi X, Zhang Y, Yin A. Huang Y, et al. Among authors: yu l. Front Genet. 2023 Feb 27;14:1032346. doi: 10.3389/fgene.2023.1032346. eCollection 2023. Front Genet. 2023. PMID: 36923788 Free PMC article.

2

[Value of Analyzing Hemoglobin A₂ by ROC Curve for Screening Thalassemia].

He TW, Yu LH, Guo H, Wang YX, DU L, Yuan TL, Zhang YX, Luo MY, Yin AH. He TW, et al. Among authors: yu lh. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Dec;24(6):1828-1832. doi: 10.7534/j.issn.1009-2137.2016.06.038. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 28024502 Chinese.

3

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: yu 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

4

A Novel Multi-Exon Deletion of PACS1 in a Three-Generation Pedigree: Supplements to PACS1 Neurodevelopmental Disorder Spectrum.

Liu Y, Ding H, Yan T, Liu L, Yu L, Huang Y, Li F, Zeng Y, Huang W, Zhang Y, Yin A. Liu Y, et al. Among authors: yu l. Front Genet. 2021 Jul 23;12:690216. doi: 10.3389/fgene.2021.690216. eCollection 2021. Front Genet. 2021. PMID: 34373684 Free PMC article.

5

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: yu l. Front Pediatr. 2021 Aug 27;9:628238. doi: 10.3389/fped.2021.628238. eCollection 2021. Front Pediatr. 2021. PMID: 34513752 Free PMC article.

6

Paternal De Novo Variant of TAOK1 in a Fetus With Structural Brain Abnormalities.

Yu L, Yang C, Shang N, Ding H, Zhu J, Zhu Y, Tan H, Zhang Y. Yu L, et al. Front Genet. 2022 Jul 19;13:836853. doi: 10.3389/fgene.2022.836853. eCollection 2022. Front Genet. 2022. PMID: 35928450 Free PMC article.

7

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: yu 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

8

A novel 1p13.2 deletion associates with neurodevelopmental disorders in a three-generation pedigree.

Yu L, Ding H, Liu M, Liu L, Zhang Q, Lu J, Guo F, Zhang Y. Yu L, et al. BMC Med Genomics. 2023 May 23;16(1):114. doi: 10.1186/s12920-023-01534-7. BMC Med Genomics. 2023. PMID: 37221554 Free PMC article.

9

Clinical utility of chromosomal microarray analysis and whole exome sequencing in foetuses with oligohydramnios.

Shi X, Ding H, Li C, Liu L, Yu L, Zhu J, Wu J. Shi X, et al. Among authors: yu l. Ann Med. 2023 Dec;55(1):2215539. doi: 10.1080/07853890.2023.2215539. Ann Med. 2023. PMID: 37243546 Free PMC article.

10

Poor outcome of pediatric B-cell acute lymphoblastic leukemia associated with high level of CRLF2 gene expression in distinct molecular subtypes.

Lin D, Yang K, Yu L, Huang L, Lai X, Wu L, Xia X, Zhang J, Zheng Q, Yang L. Lin D, et al. Among authors: yu l. Front Oncol. 2023 Nov 7;13:1256054. doi: 10.3389/fonc.2023.1256054. eCollection 2023. Front Oncol. 2023. PMID: 38023153 Free PMC article.

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