Cheng J - Search Results

1

Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency.

Ma D, Chen Y, Sun Y, Yang B, Cheng J, Huang M, Zhang J, Zhang J, Hu P, Lin Y, Jiang T, Xu Z. Ma D, et al. Among authors: cheng j. Clin Biochem. 2014 Apr;47(6):455-63. doi: 10.1016/j.clinbiochem.2014.01.019. Epub 2014 Feb 3. Clin Biochem. 2014. PMID: 24503005

2

[Development and application of a method for molecular diagnosis of 21-hydroxylase deficiency].

Ma DY, Sun Y, Chen Y, Yang B, Cheng J, Huang ML, Zhang J, Zhang JJ, Hu P, Lin Y, Jiang T, Xu ZF. Ma DY, et al. Among authors: cheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):49-54. doi: 10.3760/cma.j.issn.1003-9406.2013.01.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450479 Chinese.

3

Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA.

Ma D, Yuan Y, Luo C, Wang Y, Jiang T, Guo F, Zhang J, Chen C, Sun Y, Cheng J, Hu P, Wang J, Yang H, Yi X, Wang W, Asan, Xu Z. Ma D, et al. Among authors: cheng j. Sci Rep. 2017 Aug 7;7(1):7427. doi: 10.1038/s41598-017-06828-2. Sci Rep. 2017. PMID: 28785026 Free PMC article.

4

[Genetic analysis and prenatal diagnosis for 25 Chinese pedigrees affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].

Luo C, Jiang T, Zhang J, Li L, Sun Y, Liu G, Wang Y, Cheng J, Ma D, Xu Z. Luo C, et al. Among authors: cheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):832-835. doi: 10.3760/cma.j.issn.1003-9406.2018.06.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512157 Chinese.

5

Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.

Wang Y, Cheng Q, Meng L, Luo C, Hu H, Zhang J, Cheng J, Xu T, Jiang T, Liang D, Hu P, Xu Z. Wang Y, et al. Among authors: cheng j, cheng q. Clin Genet. 2017 Jun;91(6):849-858. doi: 10.1111/cge.12926. Epub 2016 Dec 22. Clin Genet. 2017. PMID: 27883173

6

[Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies in prenatal diagnosis].

Ma DY, Hu P, Zhang JJ, Yi L, Ji XQ, Yang C, Cheng J, Li L, Lin Y, Xu ZF. Ma DY, et al. Among authors: cheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Oct;28(5):543-7. doi: 10.3760/cma.j.issn.1003-9406.2011.05.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21983731 Chinese.

7

[Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].

Luo CY, Ma DY, Zhang JJ, Hu P, Cao L, Ji XQ, Zhou J, Liu A, Wu Y, Cheng J, Lin Y, Xu ZF. Luo CY, et al. Among authors: cheng j. Zhonghua Fu Chan Ke Za Zhi. 2013 Nov;48(11):824-7. Zhonghua Fu Chan Ke Za Zhi. 2013. PMID: 24444558 Chinese.

8

Identification of one novel CHD7 mutation in a patient from China with atypical CHARGE syndrome.

Cheng J, Ma D, Wu Y, Luo C, Huang C, Hu P, Zhang J, Jiang T, Xu Z. Cheng J, et al. Gene. 2015 Oct 25;571(2):298-302. doi: 10.1016/j.gene.2015.07.042. Epub 2015 Jul 15. Gene. 2015. PMID: 26187070

9

Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case report.

Liu G, Ma D, Cheng J, Zhang J, Luo C, Sun Y, Hu P, Wang Y, Jiang T, Xu Z. Liu G, et al. Among authors: cheng j. BMC Med Genet. 2018 Apr 12;19(1):61. doi: 10.1186/s12881-018-0567-z. BMC Med Genet. 2018. PMID: 29649982 Free PMC article.

10

Identifying Novel Copy Number Variants in Azoospermia Factor Regions and Evaluating Their Effects on Spermatogenic Impairment.

Zhou R, Cheng J, Ma D, Tan J, Wang Y, Hu P, Xu Z. Zhou R, et al. Among authors: cheng j. Front Genet. 2019 May 7;10:427. doi: 10.3389/fgene.2019.00427. eCollection 2019. Front Genet. 2019. PMID: 31134133 Free PMC article.

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