Cheng J - Search Results

1

22q11.2 microduplication in a family with recurrent fetal congenital heart disease.

Hu P, Ji X, Yang C, Zhang J, Lin Y, Cheng J, Ma D, Cao L, Yi L, Xu Z. Hu P, et al. Among authors: cheng j. Eur J Med Genet. 2011 Jul-Aug;54(4):e433-6. doi: 10.1016/j.ejmg.2011.03.009. Epub 2011 Apr 5. Eur J Med Genet. 2011. PMID: 21473936

2

[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.

3

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

4

[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.

5

[Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].

Li L, Zhou XY, Ji XQ, Yang YQ, Cao L, Zhou J, Liu A, Cheng J, Liu Y, Hu P, Xu ZF. Li L, et al. Among authors: cheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Apr;29(2):214-7. doi: 10.3760/cma.j.issn.1003-9406.2012.02.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22487837 Chinese.

6

[Prenatal diagnosis of two fetuses with de novo small supernumerary markers by single nucleotide polymorphism array based comparative genomic hybridization].

Ji XQ, Li L, Lin Y, Ma DY, Liu A, Zhang JJ, Cheng J, Zhou J, Hu P, Xu ZF. Ji XQ, et al. Among authors: cheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):510-4. doi: 10.3760/cma.j.issn.1003-9406.2012.05.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042383 Chinese.

7

Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy.

Zhou J, Tan J, Ma D, Zhang J, Cheng J, Luo C, Liu G, Wang Y, Xu Z. Zhou J, et al. Among authors: cheng j. Front Genet. 2018 Feb 13;9:43. doi: 10.3389/fgene.2018.00043. eCollection 2018. Front Genet. 2018. PMID: 29487616 Free PMC article.

8

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.

9

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.

10

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

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