Feng ZC - Search Results

1

Next-generation sequencing-based molecular diagnosis of neonatal hypotonia in Chinese Population.

Wang Y, Peng W, Guo HY, Li H, Tian J, Shi YJ, Yang X, Yang Y, Zhang WQ, Liu X, Liu GN, Deng T, Sun YM, Xing WL, Cheng J, Feng ZC. Wang Y, et al. Among authors: feng zc. Sci Rep. 2016 Jun 29;6:29088. doi: 10.1038/srep29088. Sci Rep. 2016. PMID: 27353517 Free PMC article.

2

The SEPS1 G-105A polymorphism is associated with risk of spontaneous preterm birth in a Chinese population.

Wang Y, Yang X, Zheng Y, Wu ZH, Zhang XA, Li QP, He XY, Wang CZ, Feng ZC. Wang Y, et al. Among authors: feng zc. PLoS One. 2013 Jun 11;8(6):e65657. doi: 10.1371/journal.pone.0065657. Print 2013. PLoS One. 2013. PMID: 23776519 Free PMC article.

3

A novel silent deletion, an insertion mutation and a nonsense mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.

Wang Y, Yin XJ, Han T, Peng W, Wu HL, Liu X, Feng ZC. Wang Y, et al. Among authors: feng zc. Mol Genet Genomics. 2014 Dec;289(6):1237-40. doi: 10.1007/s00438-014-0883-8. Epub 2014 Jul 4. Mol Genet Genomics. 2014. PMID: 24994558

4

A MCP-1 promoter polymorphism at G-2518A is associated with spontaneous preterm birth.

Wang Y, Zhang XA, Yang X, Wu ZH, Feng ZC. Wang Y, et al. Among authors: feng zc. Mol Genet Genomics. 2015 Feb;290(1):289-96. doi: 10.1007/s00438-014-0921-6. Epub 2014 Sep 19. Mol Genet Genomics. 2015. PMID: 25234163

5

[Detection of subtelomeric copy number variations in children with intellectual disability].

Zhu LN, Wang Y, Peng W, Ma XW, Yang X, Liu X, Feng ZC. Zhu LN, et al. Among authors: feng zc. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Dec;17(12):1273-6. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 26695663 Free article. Chinese.

6

Two novel L2HGDH mutations identified in a rare Chinese family with L-2-hydroxyglutaric aciduria.

Peng W, Ma XW, Yang X, Zhang WQ, Yan L, Wang YX, Liu X, Wang Y, Feng ZC. Peng W, et al. Among authors: feng zc. BMC Med Genet. 2018 Sep 14;19(1):167. doi: 10.1186/s12881-018-0675-9. BMC Med Genet. 2018. PMID: 30217188 Free PMC article.

7

Gene-Focused Networks Underlying Phenotypic Convergence in a Systematically Phenotyped Cohort With Heterogeneous Intellectual Disability.

Wang Y, Zhu LN, Ma XW, Yang F, Xu XL, Yang Y, Yang X, Peng W, Zhang WQ, Liang JY, Zhu WD, Jiang TJ, Zhang XL, Feng ZC. Wang Y, et al. Among authors: feng zc. Front Bioeng Biotechnol. 2020 Feb 7;8:45. doi: 10.3389/fbioe.2020.00045. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 32117926 Free PMC article.

8

Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report.

Wang Y, Chen Y, Wang SM, Liu X, Gu YN, Feng Z. Wang Y, et al. BMC Med Genet. 2020 Nov 11;21(1):222. doi: 10.1186/s12881-020-01157-0. BMC Med Genet. 2020. PMID: 33176713 Free PMC article.

9

Latency period of PROM at term and the risk of neonatal infectious diseases.

Zhuang L, Li ZK, Zhu YF, Ju R, Hua SD, Yu CZ, Li X, Zhang YP, Li L, Yu Y, Zeng W, Cui J, Chen XY, Peng JY, Li T, Feng ZC. Zhuang L, et al. Among authors: feng zc. Sci Rep. 2022 Jul 18;12(1):12275. doi: 10.1038/s41598-022-16593-6. Sci Rep. 2022. PMID: 35851306 Free PMC article.

10

[Lung ultrasound for diagnosis of neonatal atelectasis].

Liu J, Liu Y, Wang HW, Li JY, Han T, Liang J, Yang CS, Xing M, Feng ZC. Liu J, et al. Among authors: feng zc. Zhonghua Er Ke Za Zhi. 2013 Sep;51(9):644-8. Zhonghua Er Ke Za Zhi. 2013. PMID: 24330981 Chinese.

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