Meng J - Search Results

1

Generation of ZZUi008-A, a transgene-free, induced pluripotent stem cell line derived from chorionic villi cells of a fetus with Duchenne muscular dystrophy.

Zhu X, Cai A, Meng J, Liu L, Cui S, Qu S, Zhao J, Liu N, Kong X. Zhu X, et al. Among authors: meng j. Stem Cell Res. 2018 Oct;32:47-50. doi: 10.1016/j.scr.2018.07.017. Epub 2018 Jul 17. Stem Cell Res. 2018. PMID: 30172907 Free article.

2

[Mutation analyses and prenatal diagnosis in two families of X linked severe combined immunodeficiency caused by IL2RG gene novel mutation].

Kong X, Liu N, Xu X, Wu Q, Zhao Z, Bai Q, Meng J. Kong X, et al. Among authors: meng j. Zhonghua Yi Xue Za Zhi. 2014 Apr 29;94(16):1227-31. Zhonghua Yi Xue Za Zhi. 2014. PMID: 24924886 Chinese.

3

[Genetic analysis for a family affected with hemophilia type A due to a large deletion of F8 gene].

Bai N, Mei S, Liu N, Zhao Z, Meng J, Kong X. Bai N, et al. Among authors: meng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):782-785. doi: 10.3760/cma.j.issn.1003-9406.2016.06.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984605 Chinese.

4

Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2.

Xia JK, Bai ZX, Zhao XC, Meng JJ, Chen C, Kong XD. Xia JK, et al. Pediatr Neonatol. 2020 Oct;61(5):558-560. doi: 10.1016/j.pedneo.2020.04.005. Epub 2020 Apr 15. Pediatr Neonatol. 2020. PMID: 32482602 Free article. No abstract available.

5

[Genetic diagnosis for a patient with Leydig cell hypoplasia caused by two novel variants of LHCGR gene].

Xia J, Li L, Duan F, Meng J, Yan S, Li S, Ren H, Kong X. Xia J, et al. Among authors: meng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Aug 10;37(8):819-822. doi: 10.3760/cma.j.issn.1003-9406.2020.08.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32761586 Chinese.

6

[Confirmation and analysis of 2 398 positive results of cell-free fetal DNA].

Zhao JH, Dai P, Zhu RN, Shi PL, Meng JJ, Kong XD. Zhao JH, et al. Among authors: meng jj. Zhonghua Fu Chan Ke Za Zhi. 2020 Oct 25;55(10):679-684. doi: 10.3760/cma.j.cn112141-20200307-00185. Zhonghua Fu Chan Ke Za Zhi. 2020. PMID: 33120479 Chinese.

7

[Genetic screening and prenatal diagnosis in high-risk families with tuberous sclerosis complex syndrome].

Lin R, Zhao Z, Liu L, Wang C, Chen C, Liu N, Meng J, Kong X. Lin R, et al. Among authors: meng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 May 10;38(5):435-438. doi: 10.3760/cma.j.cn511374-20200325-00203. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33974250 Chinese.

8

Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome via Exome Sequencing and Low-Coverage Whole-Genome Sequencing.

Li Q, Zhu X, Wang C, Meng J, Chen D, Kong X. Li Q, et al. Among authors: meng j. Front Genet. 2021 Sep 20;12:707411. doi: 10.3389/fgene.2021.707411. eCollection 2021. Front Genet. 2021. PMID: 34616427 Free PMC article.

9

Novel Partial Exon 51 Deletion in the Duchenne Muscular Dystrophy Gene Identified via Whole Exome Sequencing and Long-Read Whole-Genome Sequencing.

Li Q, Chen Z, Xiong H, Li R, Yu C, Meng J, Shi P, Kong X. Li Q, et al. Among authors: meng j. Front Genet. 2021 Nov 26;12:762987. doi: 10.3389/fgene.2021.762987. eCollection 2021. Front Genet. 2021. PMID: 34899847 Free PMC article.

10

Case Report: A Novel Homozygous Mutation in MYF5 Due to Paternal Uniparental Isodisomy of Chromosome 12 in a Case of External Ophthalmoplegia With Rib and Vertebral Anomalies.

Li Q, Zhu X, Yu C, Shang L, Li R, Wang X, Yang Y, Meng J, Kong X. Li Q, et al. Among authors: meng j. Front Genet. 2022 Feb 3;12:780363. doi: 10.3389/fgene.2021.780363. eCollection 2021. Front Genet. 2022. PMID: 35186005 Free PMC article.

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